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Preparation. Administration. Evidence.

IV Dilution &
Medication Reference

Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements. Full monograph updates remain pending.

Version 6.4Release date 2026-11-04For healthcare professionals
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Medication reference

Naloxone

Monograph awaiting updateThis monograph will be updated in the future.

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Historical source. Current clinical review is incomplete. This monograph will be updated in the future.

Naloxone - Narcan ® (opens in a new tab)Original source URL: https://globalrph.com/dilution/naloxone-narcan/ | Retrieved 2026-11-04

Source dates, location and integrity

This historical article is separate from the reviewed claim cards. Product formulations and source dates may differ.

Original source URL
https://globalrph.com/dilution/naloxone-narcan/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:47:36.241039+00:00
Source location
div.post-content
Packaged content SHA-256
cf43fe2013715c28d2584ede148e480e095aab83b0db3076420e54736f1bf897
Original response SHA-256
585e9748ac081ea7ddb1ee912090fb495061c4354576c2fc789b86fbb1114b08
Source body SHA-256
c541eee84f814272e3dfe324bfb6c542e665e586bb04bdca6e8dd9000b32e7bf

Naloxone (Narcan ®)

The authors make no claims of the accuracy of the information contained herein; and these suggested doses and/or guidelines are not a substitute for clinical judgment. Neither GlobalRPh Inc. nor any other party involved in the preparation of this document shall be liable for any special, consequential, or exemplary damages resulting in whole or part from any user's use of or reliance upon this material. PLEASE READ THE DISCLAIMER CAREFULLY BEFORE ACCESSING OR USING THIS SITE. BY ACCESSING OR USING THIS SITE, YOU AGREE TO BE BOUND BY THE TERMS AND CONDITIONS SET FORTH IN THE DISCLAIMER.

Usual Diluents

D5W, NS

Standard Dilutions [Amount of drug] [Infusion volume] [Infusion rate]

[2 mg] [500 ml]

Fluid restricted - Higher concentrations possible:
[4 mg] [250 ml] [Titrate]
Several protocols available. See references below.

Background

The first version of this monograph was written several years ago (~ 1993). Occasionally changes or updates are added based on newly available data. Most recent update (Sept 2013):

Sample references:
[1] Source: Irwin RS, Rippe JM. Irwin and Rippe's Intensive Care Medicine. Lippincott Williams & Wilkins, 2012. (p 1656).

A continuous naloxone infusion should be considered in patients who have a positive response but require repeated bolus doses (up to 10-20 mg in some cases) because of recurrent respiratory depression...

Preparation for continuous infusion: multiply the effective bolus dose by 6.6, and then add this quantity to 1000ml NS and infuse the solution at 100 ml/hr. Titrate to maintain adequate spontaneous ventilation without precipitating acute withdrawal.

Extremely safe drug: Naloxone has been administered at dosages of 5.4 mg/kg bolus followed by infusion at 4 mg/kg for 23 hours in the treatment of acute spinal cord injury. https://www.ncbi.nlm.nih.gov/pubmed/1727165
[Note: NOT effective for this indication]

Dave's summary: assuming the effective bolus dose was in the range of 1 to 10 mg or possibly higher, the preparation would be as follows:
Range: 6.6 mg to 66 mg/1000ml
10 mg/1000 ml = 2.5 mg250ml
20 mg/1000 ml = 5 mg/250 ml
30 mg/1000 ml = 7.5 mg/250 ml
40 mg/1000ml = 10 mg/250 ml

[2] Source: Helms RA, Quan DJ (eds). Textbook of Therapeutics: Drug and Disease Management. 8th ed. Philadelphia: Lippincott Williams St Wilkins; 2006. p 82.

Naloxone has short half-life of 1 hour and its duration of action of between 30 min to up to 4 hrs is often shorter than the duration of action of the opioid.

Following reversal with bolus doses, a continous infusion of naloxone can be considered for overdoses for which repeated doses are needed for recurring toxicity.

Preparation: After reversal of respiratory depression with the bolus, the infusion is initiated at two-thirds of the bolus dose per hour. At 15 min after initiation of the infusion, half of the bolus dose is readministered. If the patient becomes symptomatic at a given rate, reverse with additional bolus doses and adjust continuous infusion rate. In adults, the naloxone concentration in D5W usually is adjusted to deliver the dose in 100 ml of solution per hour.

[3] Source: https://www.anesthesia-analgesia.org/content/100/4/953.full

Patients were randomly assigned by the hospital's investigational drug pharmacy to one of two groups using computer-generated random numbers. Group 1, the study group, received 0.25 µg · kg-1 · h-1 of naloxone by continuous infusion. The naloxone was administered by a continuous infusion pump "piggy-backed" into the patient's IV catheter. The naloxone solution was prepared in the pharmacy by mixing 2 mg of naloxone in 250 mL of 0.9% saline (final concentration = 8 µg/mL).

[4] Much higher concentrations were used in syringes: Source: Stewart JT, Warren FW, King DT, et al: Stability of ondansetron hydrochloride and 12 medications in plastic syringes. Am J Health-Syst Pharm: 1998. 55: 2630-4.

Naloxone HCL concentration: 0.133mg/mL
Diluent: Sodium chloride 0.9% (Polypropylene 35-mL syringes)
Both physically and chemically stable (no loss in potency or visible particulate formation etc) over 24hrs

[5] Product Information: NARCAN(R) injection, naloxone hcl injection. Endo Pharmaceuticals,Inc.
Dilute naloxone with normal saline (NS) or 5% dextrose in water (D5W) to a concentration of 0.004 milligrams per milliliter (mg/mL) (2 mg in 500 mL).

Stability / Miscellaneous

Dosing: Treatment of narcotic-induced respiratory depression: 0.4 to 2 mg IV / SC/ IM repeat q2 to 3 minutes prn

(if no response after 10 mg --- questionable narcotic ingestion).
IV infusion: ( 2 mg/500 ml per manufacturer)
Usual infusion rate: @ 0.4 mg/hr (100 ml/hr)-titrate to respiratory rate/ level of consciousness.

DOSAGE AND ADMINISTRATION
Naloxone Hydrochloride Injection, USP may be administered intravenously, intramuscularly, or subcutaneously. The most rapid onset of action is achieved by intravenous administration and it is recommended in emergency situations.

Since the duration of action of some opioids may exceed that of naloxone, the patient should be kept under continued surveillance and repeated doses of naloxone should be administered, as necessary.

Intravenous Infusion: Naloxone Hydrochloride Injection, USP may be diluted for intravenous infusion in 0.9% sodium chloride injection or 5% dextrose injection. The addition of 2 mg of naloxone hydrochloride in 500 mL of either solution provides a concentration of 0.004 mg/mL. Mixtures should be used within 24 hours. After 24 hours, the remaining unused solution must be discarded. The rate of administration should be titrated in accordance with the patient's response.

Naloxone Hydrochloride Injection, USP should not be mixed with preparations containing bisulfite, metabisulfite, long-chain or high molecular weight anions, or any solution having an alkaline pH. No drug or chemical agent should be added to Naloxone Hydrochloride Injection, USP unless its effect on the chemical and physical stability of the solution has first been established.

Alternatively:
Children and Adults: Continuous infusion: I.V.: If continuous infusion is required, calculate dosage/hour based on effective intermittent dose used and duration of adequate response seen, titrate dose 0.024-0.04 mg/kg/hour (higher dosages have been reported) for 2-5 days in children, adult dose typically 0.25-6.25 mg/hour (short-term infusions as high as 2.4 mg/kg/hour have been tolerated in adults during treatment for septic shock); alternatively, continuous infusion utilizes 2/3 of the initial naloxone bolus on an hourly basis; add 10 times this dose to each liter of D5W and infuse at a rate of 100 mL/hour; 1/2 of the initial bolus dose should be readministered 15 minutes after initiation of the continuous infusion to prevent a drop in naloxone levels; increase infusion rate as needed to assure adequate ventilation.

Stability:
Store at 25°C (77°F); protect from light; stable in 0.9% sodium chloride and D5W at 4 mcg/mL for 24 hours; do not mix with alkaline solutions. (Source: Lexi-drugs)

Usage in Adults:
Opioid Overdose-Known or Suspected: An initial dose of 0.4 mg to 2 mg of naloxone hydrochloride may be administered intravenously. If the desired degree of counteraction and improvement in respiratory functions is not obtained, it may be repeated at 2 to 3 minute intervals. If no response is observed after 10 mg of naloxone hydrochloride have been administered, the diagnosis of opioid induced or partial opioid induced toxicity should be questioned. Intramuscular or subcutaneous administration may be necessary if the intravenous route is not available.

Postoperative Opioid Depression: For the partial reversal of opioid depression following the use of opioids during surgery, smaller doses of naloxone hydrochloride are usually sufficient. The dose of naloxone should be titrated according to the patient's response. For the initial reversal of respiratory depression, naloxone hydrochloride should be injected in increments of 0.1 to 0.2 mg intravenously at two to three minute intervals to the desired degree of reversal, i.e., adequate ventilation and alertness without significant pain or discomfort. Larger than necessary dosage of naloxone may result in significant reversal of analgesia and increase in blood pressure. Similarly, too rapid reversal may induce nausea, vomiting, sweating or circulatory stress.

Repeat doses of naloxone may be required within one to two hour intervals depending upon the amount, type (i.e., short or long acting) and time interval since last administration of opioid. Supplemental intramuscular doses have been shown to produce a longer lasting effect.

Septic Shock: The optimal dosage of Naloxone or duration of therapy for the treatment of hypotension in septic shock patients has not been established

Source: [package insert]

Additional Pain Management / Palliative Care resources

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Open this historical article on its own

Product identifiers and clinical review status

This monograph will be updated in the future. Historical material is available where present in the original sources; full current exact-product and claim-level review remains pending.

Exact formulation, concentration, container, manufacturer, regulatory identifiers, and a reproducible label snapshot have not all been reconciled.

What remains to be completed
  • Retrievable exact-product SPL XML with version, revision, retrieval date and reproducible hash
  • Clinically reviewed, individually identified statements with two exact source mappings
  • Exact formulation, strength, container, manufacturer/labeler, application and NDC reconciliation
  • Renal-function methods and dialysis/CRRT modality review where applicable
  • Mechanism provenance, clinical source disagreements and full medication-specific safety reconciliation

Supplemental historical fields

Restored-data provenance and review notes

Source release: 2026-08-31. Current clinical review is incomplete. Original uses of current, verified, or normalized describe the historical source. They do not inherit the status of separately reviewed statements. Product formulations and source dates can differ.

Current review annotations for historical renal, dialysis, mechanism, and product fieldsSeparate renal reference: Open Renal Dosing Master (opens in a new tab)
Renal
Status
not_locally_normalized
Original classification
current_label_review_required
Entries
    General note
    Preserve the source-specific renal-function basis. An indexed CrCl table is not interchangeable with unindexed CrCl or eGFR. Generic advice to check a method does not identify the equation for a dose row.
    Dialysis
    Status
    no_local_structured_regimen
    Entries
      General note
      Named modality alone does not establish applicability. CRRT subtype, effluent rate, residual renal function, timing and interruptions require review. Historical absence is not evidence that no guidance exists.
      Mechanisms
      • Source kind
        first_look
        Local pointer
        /mechanism
        Original level
        drug_specific
        Provenance classification
        historical_drug_specific_uncorroborated
        Label derived verified
        false
        Independently corroborated
        false
        Exact label section
        Not recorded
        Original source note
        Not recorded
        Review status
        historical_unverified
        Note
        Drug-specific wording in the old file is not proof of independent corroboration or an exact label locator. Consult separately published current mechanism claims where present.
      Future update
      Status
      pending_review
      Message
      This monograph will be updated in the future as current exact-product and claim-level review is completed.
      Source unavailable
      false
      Reason
      The historical content is restored; comprehensive contemporary verification remains incomplete.
      Historical first look: uses, mechanism, dosing context, and administration

      Recovered v5.1 source content; historical, awaiting current review.

      Id
      naloxone
      Source IDH51-883396A84EF3C305B5CCF26B
      Generic name
      Naloxone
      Source IDH51-EC83C0451F620548CA388167
      Class
      Toxicology and reversal
      Source IDH51-DF4D8B898DA09DB975F09577
      Subclass
      Opioid antagonist
      Source IDH51-3BE8E3EAD2A06A186E844E37
      Primary uses
      1. Opioid-induced respiratory depression
        Source IDH51-018FBE3386EE6792CD18E0F0
      2. Postoperative opioid reversal
        Source IDH51-B0D8A0E43F9BCC18C2F3C473
      Mechanism
      Competitively blocks opioid receptors, with greatest clinical relevance at mu receptors.
      Source IDH51-95D04F641A9AA5DE003D6BA6
      Mechanism level
      drug_specific
      Source IDH51-9A75FDE32E32544881034680
      Basic dosing orientation
      Adult infusion | Existing preparation record; use current package insert for indication-specific selection | Common method: calculate hourly dose from effective bolus | Not normalized in the preparation record | See current package insert and professional guidance | IV infusion; Adult titrated reversal | Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest | Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest | Patient- and indication-specific | See current package insert | IV push
      Source IDH51-3D734F2C7DE3FC2C9371FA13
      Administration orientation
      Titrate to respiratory goal; Give over about 30 seconds and reassess; Dilute to 0.04 mg/mL for fine titration when appropriate; Give over about 30 seconds and reassess
      Source IDH51-9E9D9E6A46FD68F1837376BE
      Renal and population orientation
      Separate renal reference: Open Renal Dosing Master (opens in a new tab)Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-B833006CA09C140A1289688D
      Key safety orientation
      1. Acute withdrawal, severe pain, agitation, pulmonary edema, and arrhythmia.
        Source IDH51-59C92709969D7DB3D7BD962F
      2. Duration may be shorter than the opioid.
        Source IDH51-BCED828E830F83FAC8D2CD35
      Coverage path
      structured_local_snapshot
      Source IDH51-077FE613186279D7F2B750DD
      Coverage path label
      Structured GlobalRPh route snapshot
      Source IDH51-181036548D63DCCDF77C3220
      Legacy title
      Naloxone
      Source IDH51-369D4CB40CC611CCF307FEE8
      Review note
      First-look orientation only. Verify indication, patient population, weight basis, organ function, exact IV product, dose, concentration, compatibility, rate, and current labeling before use.
      Source IDH51-780E2093F15424D41E1E53CE
      Search text
      Naloxone Toxicology and reversal Opioid antagonist Opioid-induced respiratory depression Postoperative opioid reversal Competitively blocks opioid receptors, with greatest clinical relevance at mu receptors. Adult infusion | Existing preparation record; use current package insert for indication-specific selection | Common method: calculate hourly dose from effective bolus | Not normalized in the preparation record | See current package insert and professional guidance | IV infusion; Adult titrated reversal | Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest | Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest | Patient- and indication-specific | See current package insert | IV push Titrate to respiratory goal; Give over about 30 seconds and reassess; Dilute to 0.04 mg/mL for fine titration when appropriate; Give over about 30 seconds and reassess Renal dosing status has not been locally normalized; use the current package insert before ordering or administration. Acute withdrawal, severe pain, agitation, pulmonary edema, and arrhythmia. Duration may be shorter than the opioid. Structured GlobalRPh route snapshot
      Source IDH51-A839125B049CA4B9AB6149D5
      Official access mode
      search
      Source IDH51-851B7B03AA1370BFE85D1637
      Official search query
      Naloxone
      Source IDH51-710599E57B23BCDA77E12CB6
      Official access reason
      A source-backed DailyMed search is available; select and confirm the exact IV product.
      Source IDH51-9C80279FB71B1E3D73C82908

      No separate structured rows were bundled for dialysis, CRRT. Historical article content and source links may cover these topics.

      Historical dilution and intermittent infusion preparation

      Recovered v5.1 source content; historical, awaiting current review.

      PopulationAmountReconstitutionDiluentFinal volumeConcentrationRateStabilityNotes
      Source IDH51-1481756278D63F48FF3BCD48
      Adult infusion
      Source IDH51-5C500E04EFAD8D7AC31D374D
      Common method: calculate hourly dose from effective bolus
      Source IDH51-338EA55FCD3E7090526B553B
      Add naloxone to compatible fluid using standardized concentration.
      Source IDH51-A62D185CF788B3227A37B7F0
      NS or D5W
      Source IDH51-547D7FE86E41C7DA5ACE2266
      100 to 250 mL
      Source IDH51-D96595C7E87EE353A8614E73
      Commonly 4 to 40 mcg/mL
      Source IDH51-9C2373D42667841069489FA8
      Titrate to respiratory goal
      Source IDH51-72C9AF17A1C38E7EE7BC1B7A
      Use the shorter of current product labeling, validated stability data, and the applicable USP <797> sterility-based BUD ceiling.
      Source IDH51-29014A43EA9AFB46151F9689
      A common starting concept is about two-thirds of the effective wake-up bolus per hour, but use local protocol.
      Source IDH51-9E4625D31C0F547E9549D0E2

      Historical IV-push guidance

      Recovered v5.1 source content; historical, awaiting current review.

      PopulationDose scopeConcentrationRateStatus
      Source IDH51-DBAA4559939CF9DDF395559D
      Adult titrated reversal
      Source IDH51-2433DBF064DCF6138A9479B4
      Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest
      Source IDH51-4DD971D7288F858CEBC4FE6C
      Dilute to 0.04 mg/mL for fine titration when appropriate
      Source IDH51-959E7D13B3F63B3C24731A7D
      Give over about 30 seconds and reassess
      Source IDH51-7511C17C2E06A77E44ADD522
      Emergency/monitored use
      Source IDH51-A3E5DD02F8E0619365D7EF8F
      Source IDH51-FBA66D4018D78F6AEB7C56F8
      Pediatric
      Source IDH51-A80A261EE7E4E7C2616BE41F
      Weight-based dose
      Source IDH51-BF613291B28550DDFCA087E3
      Diluted as needed
      Source IDH51-D764F2DBEE650AB5D9B94D49
      Over about 30 seconds
      Source IDH51-51790FBDF4A47BFA55D7388D
      Pediatric emergency protocol
      Source IDH51-C5295DE5A7549A04E5204206

      Historical continuous-infusion guidance

      Recovered v5.1 source content; historical, awaiting current review.

      PopulationStandard concentrationInitial rateTitrationMaximumNotes
      Source IDH51-850DA3016E54237B107AF6B0
      Adult
      Source IDH51-D0A03015E842AC9B9240519B
      4 to 40 mcg/mL standardized concentration
      Source IDH51-79E3C1FA55AD23F15F30A3F3
      Based on effective bolus and opioid duration
      Source IDH51-88B90F853A2CD95D622499EA
      Titrate to ventilation while avoiding severe withdrawal
      Source IDH51-2A7D28D56E2D12CC40503828
      Protocol-specific
      Source IDH51-E6D2117AA7583C7FFB701FE5
      Monitor beyond discontinuation for recurrent respiratory depression.
      Source IDH51-ECE352CFF0487C526722B648

      Historical indication and population dosing

      Recovered tables and source-separated snapshots; full clinical revalidation remains pending.

      Existing dose and route snapshots

      RoutePopulationIndicationDoseIntervalDurationAdministrationSource levelNotes
      Source IDH51-95F586121009A31C8A8985A6
      IV infusion
      Source IDH51-A1B911886AA488880EF22F8D
      Adult infusion
      Source IDH51-46B40BA6974C5B846367D842
      Existing preparation record; use current package insert for indication-specific selection
      Source IDH51-B0123297BE49BB289B043708
      Common method: calculate hourly dose from effective bolus
      Source IDH51-053C915BE6B43E1A11A07435
      Not normalized in the preparation record
      Source IDH51-3A041E4083447E00D5DF33C9
      See current package insert and professional guidance
      Source IDH51-01E37192A9E5A9AFC6ED16BD
      Titrate to respiratory goal
      Source IDH51-E0C0C8E6D2EA6D4AD8151080
      Existing GlobalRPh structured preparation snapshot
      Source IDH51-939EE5DDD1C5DF19CC5217F6
      A common starting concept is about two-thirds of the effective wake-up bolus per hour, but use local protocol.
      Source IDH51-DAC9C28C66895A1893803AE3
      Source IDH51-8C421615FD67A00DB9D526DC
      IV push
      Source IDH51-7087B28F0052BBE9C2F4C8C5
      Adult titrated reversal
      Source IDH51-FEA3DFBE90005CE978F4376D
      Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest
      Source IDH51-AED635EB620C9C9E70F7B27A
      Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest
      Source IDH51-BEB2CE8D463D1899859BD27B
      Patient- and indication-specific
      Source IDH51-BC6124861BF44061D20C5ED1
      See current package insert
      Source IDH51-06EAAB98DBAA46D5E8917CE2
      Give over about 30 seconds and reassess
      Source IDH51-86A152EB7C37FFCCF1A42C6E
      Existing GlobalRPh IV push snapshot
      Source IDH51-FE23C60055ADB1F0A60BD52B
      Emergency/monitored use
      Source IDH51-B07686E3F0C23A05D8CEDA05
      Source IDH51-A40C6AB72EEFE57272451A9A
      IV push
      Source IDH51-E30FD3E95C247186249EF247
      Pediatric
      Source IDH51-11D210748FC7F8B9556DDB0E
      Weight-based dose
      Source IDH51-EADFADE509E80E8DC1E773CF
      Weight-based dose
      Source IDH51-5651A07D8257A87A8E01CB5E
      Patient- and indication-specific
      Source IDH51-2050BD50E3C49B6AC1188E2F
      See current package insert
      Source IDH51-6AB5A5281ABA7BC324994DD7
      Over about 30 seconds
      Source IDH51-23FD7F5B3997E92A7DBD6D2B
      Existing GlobalRPh IV push snapshot
      Source IDH51-E4C56CD5948F58969268037E
      Pediatric emergency protocol
      Source IDH51-44970162B7B1716B5DBCDAEA
      Source IDH51-CE786BD77432CC591C0F1B53
      Continuous IV infusion
      Source IDH51-BD6CD02E014CA905F516218E
      Adult
      Source IDH51-D3B264D38CB9B2A209491EFA
      Existing continuous-infusion record
      Source IDH51-D0E53EF0B8B6BEC5B991D68B
      Based on effective bolus and opioid duration
      Source IDH51-40271F8550303EC1F8762062
      Continuous infusion; titration-specific
      Source IDH51-98D7F063B4EF47C30D7184C3
      Clinical-response dependent
      Source IDH51-D07E33BCBE3FE9EEA14A85F1
      Titrate to ventilation while avoiding severe withdrawal
      Source IDH51-7B8241532B2DE0F978E978F9
      Existing GlobalRPh continuous-infusion snapshot
      Source IDH51-2337D5DEC430A5157383ADCC
      Protocol-specific Monitor beyond discontinuation for recurrent respiratory depression.
      Source IDH51-EC9DAAF1B6DDF653D751277E

      Historical renal-function guidance

      Recovered v5.1 source content; historical, awaiting current review.

      Separate renal reference: Open Renal Dosing Master (opens in a new tab)
      Classification
      current_label_review_required
      Source IDH51-60BC23E8B0F78698D0FD5D7B
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-54AF30F782746EEF37EC080F
      Method note
      Use the renal function estimate and body-size convention specified by the selected label or institutional protocol. Do not interchange Cockcroft-Gault CrCl, indexed eGFR, and de-indexed eGFR without confirming the dosing source.
      Source IDH51-65A9CF3F4C3746A131E1C8ED

      Historical Common IV uses

      Recovered v5.1 source content; historical, awaiting current review.

      1. Opioid-induced respiratory depression
        Source IDH51-DD8F44610C36337ABE55B3E5
      2. Postoperative opioid reversal
        Source IDH51-059AAD6D12293BD8005F3BEF

      Historical Warnings and safeguards

      Recovered v5.1 source content; historical, awaiting current review.

      1. Acute withdrawal, severe pain, agitation, pulmonary edema, and arrhythmia.
        Source IDH51-5F561CF0FBABADED6C35CBFA
      2. Duration may be shorter than the opioid.
        Source IDH51-42E550C961E274844EBFF89D

      Historical Monitoring

      Recovered v5.1 source content; historical, awaiting current review.

      1. Continuous respiratory and sedation assessment
        Source IDH51-B1C13E7491B1B30CBD15C589
      2. Recurrent toxicity
        Source IDH51-7D5BCE20686B2D6C0317CD0D
      3. Withdrawal and pain
        Source IDH51-2EBC119C0D77B85437417084
      Other recovered source fields and original editorial metadata

      Original status words such as current, verified, or normalized describe the historical source release. They do not change the clinical review status of this release.

      Catalog source fields

      Id
      naloxone
      Source IDH51-5F73476E7CDA29C50C1E668D
      Generic name
      Naloxone
      Source IDH51-3940D404A1C2432D92290883
      Brand names
      1. Narcan
        Source IDH51-35A1E07F863DAEFFA7CA9415
      Class
      Toxicology and reversal
      Source IDH51-D899F65C5AD59DEA460D9782
      Subclass
      Opioid antagonist
      Source IDH51-2B63CCDDD8B5EFB5DB881723
      Summary
      Opioid reversal agent best titrated to adequate ventilation rather than complete arousal when ongoing analgesia is desired; recurrent toxicity may require infusion.
      Source IDH51-A02ED9D43A0779629FA2A742
      Populations
      1. Adult
        Source IDH51-0C707B599AB9A56EEEA5933F
      2. Pediatric
        Source IDH51-1E9BDB45239448AA41DE2D8C
      3. Neonatal selected use
        Source IDH51-8B99165F871AFF2A32F7A359
      Evidence tier
      Core reference - verify current label
      Source IDH51-CEFE200204181DAD58E424E6
      High alert
      true
      Source IDH51-712468E1C4B59F678A6D7DD8
      Hazardous
      false
      Source IDH51-5BEA7F274DDE2394DA4EBE96
      Status
      Active
      Source IDH51-77608C3D5F7826DDC225736E
      Reviewed
      2026-08-29
      Source IDH51-94F4C59F2DD0B226A0FD4A68
      Version added
      1.2
      Source IDH51-E9D9F8E5D190BA4E61EABD4B
      Sources
      LabelUrlKind
      Source IDH51-06F4E3BE2E2CCF32306E99AB
      DailyMed label search
      Source IDH51-6DB82C4FF7F4BB4794027EED
      https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Naloxone (opens in a new tab)
      Source IDH51-D40A6000DD9B28F46B774708
      Primary
      Source IDH51-C9A0BD9BCD0E14044BFDEE18
      Source IDH51-5EC20F43EC384F4F42553BFD
      GlobalRPh legacy IV dilution monograph
      Source IDH51-5D342BA9CA6B1B79A7B49477
      legacy:auto
      Source IDH51-59448D8AEC16FBAC04FA56BF
      Legacy
      Source IDH51-C28345C45390F203470E600C
      Legacy title
      Naloxone
      Source IDH51-AE05BA40F53ED03197D747E9
      Clinical release verification
      Audit version
      3.4
      Source IDH51-13752BCCC3399ED80FA43FEF
      Audited on
      2026-08-30
      Source IDH51-B05CE4AA62885BB4CAE67531
      Level
      amber
      Source IDH51-6B93D59F1FB979F8BB5D0A25
      Release gate
      trusted_professional_source_present_exact_label_unconfirmed
      Source IDH51-1692537F41772DEE60AEAEF6
      Exact current label candidate
      false
      Source IDH51-942440AEE5BF1CD4DD802EEB
      Numeric support ratio
      0
      Source IDH51-B9B1A691AA07DD1FC1DEE01E
      Reference url count
      1
      Source IDH51-ACD073921297B2566D6F9B74
      Broken reference count
      0
      Source IDH51-8C936F3C1A98558B6F3642E0
      Point of use confirmation required
      true
      Source IDH51-C988BA2F53027FE550275778
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-9A29307FB9828CF7DE739573
      Dailymed search url
      https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Naloxone (opens in a new tab)
      Source IDH51-D6D9CD94D227587CEAF9740A

      Dosing source fields

      Id
      naloxone
      Source IDH51-2A154EF844C7427B114EDBD4
      Generic name
      Naloxone
      Source IDH51-0CB2AC416E1E437361071348
      Coverage status
      direct_official_label_access_plus_local_snapshot
      Source IDH51-C70CD60A30363DFAC823FCD9
      Package insert
      Query name
      Naloxone
      Source IDH51-AC0CE00E5AEC1149711E92BF
      Product and route must match
      true
      Source IDH51-6793FA58E638F8FB3BFF07CA
      Live current label enabled
      false
      Source IDH51-1359314E7599F381F27136A3
      Source priority
      Reviewed local summary when available, then a verified DailyMed label or product search when available, followed by professional references and institutional policy.
      Source IDH51-D9E1607690FABBF7B0A1C1C8
      Direct official label access enabled
      true
      Source IDH51-434B539B63B99E4DFE81A3F3
      Outbound server request required
      false
      Source IDH51-6BE49B3B1729D176F697385A
      Local summary status
      not_bundled
      Source IDH51-749AF23CC5D7C3BF22CCF64C
      Clinical review
      Locally normalized
      false
      Source IDH51-F4BF93B18EED11FE3898C54A
      Reviewed
      2026-08-29
      Source IDH51-7F4E9AC9DC8260AD2819104C
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-E1693C7928EDF78EAF74F6D8
      Clinical release verification
      Audit version
      3.4
      Source IDH51-514BDBC700036606C2FA29AC
      Audited on
      2026-08-30
      Source IDH51-3AD967156B35E13976E7B3FC
      Level
      amber
      Source IDH51-1FDAD994A2DD2310C449DF78
      Release gate
      trusted_professional_source_present_exact_label_unconfirmed
      Source IDH51-7140FC8CB9EC5EE859EB872E
      Exact current label candidate
      false
      Source IDH51-255415978F497468EEBB8285
      Numeric support ratio
      0
      Source IDH51-2AA2C96817981F5A4518B6AE
      Reference url count
      1
      Source IDH51-9EAC06D9EEF47C902E3829B1
      Broken reference count
      0
      Source IDH51-0241A4D0125D3CDB795A0F07
      Point of use confirmation required
      true
      Source IDH51-FAD7159710544B38B9C88A20
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-06E29AAF3A6558ECA5F53EA4
      Dailymed search url
      https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Naloxone (opens in a new tab)
      Source IDH51-BDB249D43B852834A93D97AC
      Historical preparation assessment

      Recovered v5.1 source content; historical, awaiting current review.

      Id
      naloxone
      Source IDH51-06D2AF4D48858C55779BE39A
      Name
      Naloxone
      Source IDH51-B443A73546DDBC25B71EC0A1
      Brands
      Narcan
      Source IDH51-522B455BBEB6D04786179CDF
      Therapeutic class
      Toxicology and reversal
      Source IDH51-0C5B9D77EAE634367C97D32B
      Review version
      3.1
      Source IDH51-51088D65DF003182A33F5E4D
      Review date
      2026-08-30
      Source IDH51-E1B4113D68F24E20681982EC
      Release status
      structured_record_current_label_not_confirmed
      Source IDH51-6F811717254730927C574D85
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-5026FAED22D72AD5F28CBEE4
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-14BFEC63BE481C663B18F685
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-4493EFAC0D9B4F405BBC86D8
      Reconstitution concentration
      Add naloxone to compatible fluid using standardized concentration.
      Source IDH51-FE73D5DD09A1388594CDCF26
      Maximum or recommended final concentration
      4 to 40 mcg/mL standardized concentration
      Source IDH51-58FD939CD1CE4B928BF601C9
      Appropriate standardized containers
      100 to 250 mL
      Source IDH51-268B76B05DD7662C8328F7BF
      Adult dosing range
      Common method: calculate hourly dose from effective bolus Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest Weight-based dose Based on effective bolus and opioid duration Small increments such as 0.04 mg in opioid-dependent patients; larger doses for apnea or arrest Weight-based dose
      Source IDH51-A64DE5A3F48589593FF53EE7
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-BE871A1AC531629DF4754F59
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-BF6B24E3C04EB49F1DD07E3B
      Infusion time
      Titrate to respiratory goal Give over about 30 seconds and reassess Over about 30 seconds Based on effective bolus and opioid duration
      Source IDH51-76A1BDFD17DEC4C123755091
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-E459400858D3CE4C9EA72C37
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-DC4568FEF539710EAB0A293F
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-9900509CE9CBD94BA3D2AD85
      Reconstitution concentration
      Primary
      existing_structured_record
      Source IDH51-26DE48A4B952BE82E75E86FB
      Maximum or recommended final concentration
      Primary
      existing_structured_record
      Source IDH51-2EE4C46D06BAB049A3F3DE30
      Appropriate standardized containers
      Primary
      existing_structured_record
      Source IDH51-4FA81D342671441E29201254
      Adult dosing range
      Primary
      existing_structured_record
      Source IDH51-460AC2AE669A09E0C39ED039
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-6F9E24BB1718E76848562352
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-2BAA4C07D7EEEA5BC8700F52
      Infusion time
      Primary
      existing_structured_record
      Source IDH51-62384C713C9C3A4F9109C3CB
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-1DCC4BABBAB1A880BE34A20E
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-4C4217FC2B0F4F9833ADEE9E
      Population applicability
      Adult
      Applicability
      supported_or_source_present
      Source IDH51-686EE7AB4B864D24DBB7C136
      Guide generation allowed
      true
      Source IDH51-8F8A17D9E1DBC46788B1B639
      Pediatric
      Applicability
      supported_or_source_present
      Source IDH51-A0F32E29BB0F1F9D132B49B4
      Guide generation allowed
      false
      Source IDH51-DECBF81FE9FAA99FD3551588
      Neonatal
      Applicability
      supported_or_source_present
      Source IDH51-7BEB6A531CE534F4502FEC1C
      Guide generation allowed
      false
      Source IDH51-1C18ADEE81DE99460B9F9773
      Route presence
      Structured dilution
      true
      Source IDH51-F127E93CF413B0FBB95FBECB
      Iv push
      true
      Source IDH51-F15EFDA54D0CF26DBD43A5F9
      Continuous infusion
      true
      Source IDH51-B8965B988BA90BA87834AC81
      Pediatric source
      true
      Source IDH51-F7F5914B3D7FCE31F8FC959D
      Neonatal source
      true
      Source IDH51-85FB67D21B69B0F993E7EA3A
      Legacy reference
      Status
      not_available
      Source IDH51-FCE359449823A05FCC9F9520
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-A6A6856F35234589EE45F967
      Concentration values detected
      LowHighUnitText
      Source IDH51-2C01BECADB3A08420468D99B
      4
      Source IDH51-2F8AF46FC653F00B09791C13
      40
      Source IDH51-C24789947CF9A9D234FB03A0
      mcg
      Source IDH51-D95CD51A1DCADA842511E78D
      4 to 40 mcg/mL
      Source IDH51-8ECAC166161BB3DC3545D64B
      Source files
      1. catalog.json
        Source IDH51-025A69A3BA1D406E3F49C201
      2. dosing.json
        Source IDH51-361F600610F4D15CAE7E77A2
      3. legacy-map.json
        Source IDH51-68F78CAB0DDE4A7179DC9521
      4. new-in-v1.2.json
        Source IDH51-0B0CF644C82A80EA9580A4D1
      Clinical release note
      Preparation instructions are released only at the evidence level shown. Legacy content remains visibly separate. Exact product, NDC, route, current labeling, and institutional policy must be confirmed.
      Source IDH51-D9AC1CAC8427E3881858B15E
      Historical statement IDs and source locations

      These IDs identify recovered source units. They are not evidence-qualified clinical claims.

      Historical IDOriginal source locationStatus
      H51-5F73476E7CDA29C50C1E668Dcatalog.json
      /records/175/id
      Historical; current review incomplete
      H51-3940D404A1C2432D92290883catalog.json
      /records/175/generic_name
      Historical; current review incomplete
      H51-35A1E07F863DAEFFA7CA9415catalog.json
      /records/175/brand_names/0
      Historical; current review incomplete
      H51-D899F65C5AD59DEA460D9782catalog.json
      /records/175/class
      Historical; current review incomplete
      H51-2B63CCDDD8B5EFB5DB881723catalog.json
      /records/175/subclass
      Historical; current review incomplete
      H51-A02ED9D43A0779629FA2A742catalog.json
      /records/175/summary
      Historical; current review incomplete
      H51-DD8F44610C36337ABE55B3E5catalog.json
      /records/175/common_uses/0
      Historical; current review incomplete
      H51-059AAD6D12293BD8005F3BEFcatalog.json
      /records/175/common_uses/1
      Historical; current review incomplete
      H51-1481756278D63F48FF3BCD48catalog.json
      /records/175/preparations/0
      Historical; current review incomplete
      H51-5C500E04EFAD8D7AC31D374Dcatalog.json
      /records/175/preparations/0/population
      Historical; current review incomplete
      H51-338EA55FCD3E7090526B553Bcatalog.json
      /records/175/preparations/0/amount
      Historical; current review incomplete
      H51-A62D185CF788B3227A37B7F0catalog.json
      /records/175/preparations/0/reconstitution
      Historical; current review incomplete
      H51-547D7FE86E41C7DA5ACE2266catalog.json
      /records/175/preparations/0/diluent
      Historical; current review incomplete
      H51-D96595C7E87EE353A8614E73catalog.json
      /records/175/preparations/0/final_volume
      Historical; current review incomplete
      H51-9C2373D42667841069489FA8catalog.json
      /records/175/preparations/0/concentration
      Historical; current review incomplete
      H51-72C9AF17A1C38E7EE7BC1B7Acatalog.json
      /records/175/preparations/0/rate
      Historical; current review incomplete
      H51-29014A43EA9AFB46151F9689catalog.json
      /records/175/preparations/0/stability
      Historical; current review incomplete
      H51-9E4625D31C0F547E9549D0E2catalog.json
      /records/175/preparations/0/notes
      Historical; current review incomplete
      H51-DBAA4559939CF9DDF395559Dcatalog.json
      /records/175/iv_push/0
      Historical; current review incomplete
      H51-2433DBF064DCF6138A9479B4catalog.json
      /records/175/iv_push/0/population
      Historical; current review incomplete
      H51-4DD971D7288F858CEBC4FE6Ccatalog.json
      /records/175/iv_push/0/dose_scope
      Historical; current review incomplete
      H51-959E7D13B3F63B3C24731A7Dcatalog.json
      /records/175/iv_push/0/concentration
      Historical; current review incomplete
      H51-7511C17C2E06A77E44ADD522catalog.json
      /records/175/iv_push/0/rate
      Historical; current review incomplete
      H51-A3E5DD02F8E0619365D7EF8Fcatalog.json
      /records/175/iv_push/0/status
      Historical; current review incomplete
      H51-14B0E322E5350EFBFB74998Dcatalog.json
      /records/175/iv_push/0/notes
      Historical; current review incomplete
      H51-FBA66D4018D78F6AEB7C56F8catalog.json
      /records/175/iv_push/1
      Historical; current review incomplete
      H51-A80A261EE7E4E7C2616BE41Fcatalog.json
      /records/175/iv_push/1/population
      Historical; current review incomplete
      H51-BF613291B28550DDFCA087E3catalog.json
      /records/175/iv_push/1/dose_scope
      Historical; current review incomplete
      H51-D764F2DBEE650AB5D9B94D49catalog.json
      /records/175/iv_push/1/concentration
      Historical; current review incomplete
      H51-51790FBDF4A47BFA55D7388Dcatalog.json
      /records/175/iv_push/1/rate
      Historical; current review incomplete
      H51-C5295DE5A7549A04E5204206catalog.json
      /records/175/iv_push/1/status
      Historical; current review incomplete
      H51-2D805015B5D4716BF1BFC4A9catalog.json
      /records/175/iv_push/1/notes
      Historical; current review incomplete
      H51-850DA3016E54237B107AF6B0catalog.json
      /records/175/continuous_infusions/0
      Historical; current review incomplete
      H51-D0A03015E842AC9B9240519Bcatalog.json
      /records/175/continuous_infusions/0/population
      Historical; current review incomplete
      H51-79E3C1FA55AD23F15F30A3F3catalog.json
      /records/175/continuous_infusions/0/standard_concentration
      Historical; current review incomplete
      H51-88B90F853A2CD95D622499EAcatalog.json
      /records/175/continuous_infusions/0/initial_rate
      Historical; current review incomplete
      H51-2A7D28D56E2D12CC40503828catalog.json
      /records/175/continuous_infusions/0/titration
      Historical; current review incomplete
      H51-E6D2117AA7583C7FFB701FE5catalog.json
      /records/175/continuous_infusions/0/maximum
      Historical; current review incomplete
      H51-ECE352CFF0487C526722B648catalog.json
      /records/175/continuous_infusions/0/notes
      Historical; current review incomplete
      H51-5F561CF0FBABADED6C35CBFAcatalog.json
      /records/175/warnings/0
      Historical; current review incomplete
      H51-42E550C961E274844EBFF89Dcatalog.json
      /records/175/warnings/1
      Historical; current review incomplete
      H51-B1C13E7491B1B30CBD15C589catalog.json
      /records/175/monitoring/0
      Historical; current review incomplete
      H51-7D5BCE20686B2D6C0317CD0Dcatalog.json
      /records/175/monitoring/1
      Historical; current review incomplete
      H51-2EBC119C0D77B85437417084catalog.json
      /records/175/monitoring/2
      Historical; current review incomplete
      H51-0C707B599AB9A56EEEA5933Fcatalog.json
      /records/175/populations/0
      Historical; current review incomplete
      H51-1E9BDB45239448AA41DE2D8Ccatalog.json
      /records/175/populations/1
      Historical; current review incomplete
      H51-8B99165F871AFF2A32F7A359catalog.json
      /records/175/populations/2
      Historical; current review incomplete
      H51-CEFE200204181DAD58E424E6catalog.json
      /records/175/evidence_tier
      Historical; current review incomplete
      H51-712468E1C4B59F678A6D7DD8catalog.json
      /records/175/high_alert
      Historical; current review incomplete
      H51-5BEA7F274DDE2394DA4EBE96catalog.json
      /records/175/hazardous
      Historical; current review incomplete
      H51-77608C3D5F7826DDC225736Ecatalog.json
      /records/175/status
      Historical; current review incomplete
      H51-94F4C59F2DD0B226A0FD4A68catalog.json
      /records/175/reviewed
      Historical; current review incomplete
      H51-E9D9F8E5D190BA4E61EABD4Bcatalog.json
      /records/175/version_added
      Historical; current review incomplete
      H51-06F4E3BE2E2CCF32306E99ABcatalog.json
      /records/175/sources/0
      Historical; current review incomplete
      H51-6DB82C4FF7F4BB4794027EEDcatalog.json
      /records/175/sources/0/label
      Historical; current review incomplete
      H51-D40A6000DD9B28F46B774708catalog.json
      /records/175/sources/0/url
      Historical; current review incomplete
      H51-C9A0BD9BCD0E14044BFDEE18catalog.json
      /records/175/sources/0/kind
      Historical; current review incomplete
      H51-5EC20F43EC384F4F42553BFDcatalog.json
      /records/175/sources/1
      Historical; current review incomplete
      H51-5D342BA9CA6B1B79A7B49477catalog.json
      /records/175/sources/1/label
      Historical; current review incomplete
      H51-59448D8AEC16FBAC04FA56BFcatalog.json
      /records/175/sources/1/url
      Historical; current review incomplete
      H51-C28345C45390F203470E600Ccatalog.json
      /records/175/sources/1/kind
      Historical; current review incomplete
      H51-AE05BA40F53ED03197D747E9catalog.json
      /records/175/legacy_title
      Historical; current review incomplete
      H51-13752BCCC3399ED80FA43FEFcatalog.json
      /records/175/clinical_release_verification/audit_version
      Historical; current review incomplete
      H51-B05CE4AA62885BB4CAE67531catalog.json
      /records/175/clinical_release_verification/audited_on
      Historical; current review incomplete
      H51-6B93D59F1FB979F8BB5D0A25catalog.json
      /records/175/clinical_release_verification/level
      Historical; current review incomplete
      H51-1692537F41772DEE60AEAEF6catalog.json
      /records/175/clinical_release_verification/release_gate
      Historical; current review incomplete
      H51-942440AEE5BF1CD4DD802EEBcatalog.json
      /records/175/clinical_release_verification/exact_current_label_candidate
      Historical; current review incomplete
      H51-4CAB95CCDF9B6FD9DD505ED5catalog.json
      /records/175/clinical_release_verification/selected_setid
      Historical; current review incomplete
      H51-67CF5D37E5515DA1D05B698Ccatalog.json
      /records/175/clinical_release_verification/selected_label_title
      Historical; current review incomplete
      H51-B9B1A691AA07DD1FC1DEE01Ecatalog.json
      /records/175/clinical_release_verification/numeric_support_ratio
      Historical; current review incomplete
      H51-ACD073921297B2566D6F9B74catalog.json
      /records/175/clinical_release_verification/reference_url_count
      Historical; current review incomplete
      H51-8C936F3C1A98558B6F3642E0catalog.json
      /records/175/clinical_release_verification/broken_reference_count
      Historical; current review incomplete
      H51-C988BA2F53027FE550275778catalog.json
      /records/175/clinical_release_verification/point_of_use_confirmation_required
      Historical; current review incomplete
      H51-9A29307FB9828CF7DE739573catalog.json
      /records/175/clinical_release_verification/note
      Historical; current review incomplete
      H51-D6D9CD94D227587CEAF9740Acatalog.json
      /records/175/clinical_release_verification/dailymed_search_url
      Historical; current review incomplete
      H51-2A154EF844C7427B114EDBD4dosing.json
      /records/175/id
      Historical; current review incomplete
      H51-0CB2AC416E1E437361071348dosing.json
      /records/175/generic_name
      Historical; current review incomplete
      H51-C70CD60A30363DFAC823FCD9dosing.json
      /records/175/coverage_status
      Historical; current review incomplete
      H51-AC0CE00E5AEC1149711E92BFdosing.json
      /records/175/package_insert/query_name
      Historical; current review incomplete
      H51-FB8A049123940F7DE0CE19F7dosing.json
      /records/175/package_insert/preferred_setid
      Historical; current review incomplete
      H51-6793FA58E638F8FB3BFF07CAdosing.json
      /records/175/package_insert/product_and_route_must_match
      Historical; current review incomplete
      H51-1359314E7599F381F27136A3dosing.json
      /records/175/package_insert/live_current_label_enabled
      Historical; current review incomplete
      H51-D9E1607690FABBF7B0A1C1C8dosing.json
      /records/175/package_insert/source_priority
      Historical; current review incomplete
      H51-434B539B63B99E4DFE81A3F3dosing.json
      /records/175/package_insert/direct_official_label_access_enabled
      Historical; current review incomplete
      H51-6BE49B3B1729D176F697385Adosing.json
      /records/175/package_insert/outbound_server_request_required
      Historical; current review incomplete
      H51-749AF23CC5D7C3BF22CCF64Cdosing.json
      /records/175/package_insert/local_summary_status
      Historical; current review incomplete
      H51-60BC23E8B0F78698D0FD5D7Bdosing.json
      /records/175/renal/classification
      Historical; current review incomplete
      H51-54AF30F782746EEF37EC080Fdosing.json
      /records/175/renal/summary
      Historical; current review incomplete
      H51-65A9CF3F4C3746A131E1C8EDdosing.json
      /records/175/renal/method_note
      Historical; current review incomplete
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