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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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Pentobarbital

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.

Pentobarbital ( Nembutal ®) (opens in a new tab)Original source URL: https://globalrph.com/dilution/pentobarbital-nembutal/ | 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/pentobarbital-nembutal/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:47:07.229110+00:00
Source location
div.post-content
Packaged content SHA-256
5a017e773d01590a1316156cb2064120e535de1fa1da9b49dc8803d724c166ae
Original response SHA-256
46d0c8e2fb681d5cc3de251a8cb00bcef0b68df04a008f8e49675595ccb0f4d1
Source body SHA-256
ecd6b216d559e4d85bbfb245f7d2bc3c154db18d524c4c6b2101c314494cf669

Pentobarbital ( Nembutal ®)

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

NS, D5W

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

Maximum rate: 50 mg/min
[100 mg] [50 ml]
[500 - 2000 mg] [250 ml](Concentrations from 0.5 to 8 mg/ml appear to be stable)
Infusion rate: As directed.

Stability / Miscellaneous

EXP: 12 to 24 hrs (RT) variable (Review specialized reference for additional info).
Label: Do not refrigerate.Onset: 15-60 min
Duration:
(Oral): 1-4 hrs (IV): 15 min

May be given deep IM (max 250mg per site) or by slow IV injection. Note: can be given IV undiluted.

Dosing:
Hypnotic (Adult):
Oral: 100-200mg qhs.
IM: 150-200mg.
IV: Initially 100mg, may repeat q1-3min up to 200-500mg total dose. Rectal: 120-200mg at bedtime.

Preoperative sedation: IM: 150-200 mg.

Barbiturate coma in head injury patients: IV loading dose of 5-10 mg/kg over 1 to 2 hours. Maintenance: Initial: 1 mg/kg/hr; may increase to 2-3 mg/kg/hr. Monitor for dose-dependent cardiovascular and respiratory depression. Maintain serum concentration at 2-4 mg/dl.

Supplied: 50mg/ml-1ml, 2 ml, 20ml, 50ml. (C-II)

DOSAGE AND ADMINISTRATION
Dosages of barbiturates must be individualized with full knowledge of their particular characteristics and recommended rate of administration. Factors of consideration are the patient's age, weight, and condition. Parenteral routes should be used only when oral administration is impossible or impractical.

Intramuscular Administration
IM injection of the sodium salts of barbiturates should be made deeply into a large muscle, and a volume of 5 mL should not be exceeded at any one site because of possible tissue irritation. After IM injection of a hypnotic dose, the patient's vital signs should be monitored. The usual adult dosage of NEMBUTAL Sodium Solution is 150 to 200 mg as a single IM injection; the recommended pediatric dosage ranges from 2 to 6 mg/kg as a single IM injection not to exceed 100 mg.

Intravenous Administration
NEMBUTAL Sodium Solution should not be admixed with any other medication or solution. IV injection is restricted to conditions in which other routes are not feasible, either because the patient is unconscious (as in cerebral hemorrhage, eclampsia, or status epilepticus), or because the patient resists (as in delirium), or because prompt action is imperative. Slow IV injection is essential, and patients should be carefully observed during administration. This requires that blood pressure, respiration, and cardiac function be maintained, vital signs be recorded, and equipment for resuscitation and artificial ventilation be available. The rate of IV injection should not exceed 50 mg/min for pentobarbital sodium.

There is no average intravenous dose of NEMBUTAL Sodium Solution (pentobarbital sodium injection) that can be relied on to produce similar effects in different patients. The possibility of overdose and respiratory depression is remote when the drug is injected slowly in fractional doses.

A commonly used initial dose for the 70 kg adult is 100 mg. Proportional reduction in dosage should be made for pediatric or debilitated patients. At least one minute is necessary to determine the full effect of intravenous pentobarbital. If necessary, additional small increments of the drug may be given up to a total of from 200 to 500 mg for normal adults.

Anticonvulsant use
In convulsive states, dosage of NEMBUTAL Sodium Solution should be kept to a minimum to avoid compounding the depression which may follow convulsions. The injection must be made slowly with due regard to the time required for the drug to penetrate the blood-brain barrier.

Special patient population
Dosage should be reduced in the elderly or debilitated because these patients may be more sensitive to barbiturates. Dosage should be reduced for patients with impaired renal function or hepatic disease.

Inspection
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution containers permit. Solutions for injection showing evidence of precipitation should not be used.

HOW SUPPLIED
NEMBUTAL Sodium Solution (pentobarbital sodium injection, USP) is available in the following sizes: 20-mL multiple-dose vial, 1 g per vial (NDC 67386- 501-52); and 50-mL multiple-dose vial, 2.5 g per vial (NDC 67386-501-55).

Manufactured by
Hospira, Inc.
Lake Forest, Illinois 60045 U.S.A.
For:
OVATION Pharmaceuticals, Inc.
Deerfield, Illinois, U.S.A. 60015

Source: [package insert]

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
      pentobarbital
      Source IDH51-0F6584256CC6B055902DB24B
      Generic name
      Pentobarbital
      Source IDH51-7BB0BED9E3A7949CEBA864A7
      Class
      Sedation, analgesia, and anesthesia
      Source IDH51-DB2BE7F29ABAF9BF94966F8A
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-387775CE8A675923E6CFD442
      Primary uses
      1. Analgesia, sedation, induction, or peri-procedural therapy depending on the named agent and monitoring environment.
        Source IDH51-F9820C6815A6B405F6229BDB
      Mechanism
      Enhances GABA-A receptor inhibition, mainly by prolonging chloride-channel opening.
      Source IDH51-D3B513E47058CF26DCD0C7D4
      Mechanism level
      drug_specific
      Source IDH51-704E62EEE94789F2B2125889
      Basic dosing orientation
      The existing GlobalRPh dose and preparation quick reference loads automatically below. Treat it as historical continuity, then confirm the exact current DailyMed label, population, indication, renal function, and institutional policy.
      Source IDH51-7A104DB4B5191BF01CE01018
      Administration orientation
      Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required.
      Source IDH51-85FC58E7B1A1C61C2A513561
      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-BA4F22490249042CC0C4FD04
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-41AFAC2B8B047C1A7F26FEB9
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-07BD586626F18987FFBD440F
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-6A4D4A4C51DC9A0F20C531A7
      Legacy title
      Pentobarbital
      Source IDH51-3E526E42EEF51F078F102623
      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-BD5B91787A9BAEBA43087157
      Search text
      Pentobarbital Sedation, analgesia, and anesthesia Legacy GlobalRPh directory entry Analgesia, sedation, induction, or peri-procedural therapy depending on the named agent and monitoring environment. Enhances GABA-A receptor inhibition, mainly by prolonging chloride-channel opening. The existing GlobalRPh dose and preparation quick reference loads automatically below. Treat it as historical continuity, then confirm the exact current DailyMed label, population, indication, renal function, and institutional policy. Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required. Renal dosing status has not been locally normalized; use the current package insert before ordering or administration. Legacy content must be reconciled against current labeling and institutional policy before clinical use. Automatic legacy GlobalRPh quick reference
      Source IDH51-E4357F9BC9A46808F6CF1CEA
      Official access mode
      none
      Source IDH51-2867E718BEC3204FE0210F78
      Official access reason
      No source-backed DailyMed action has been verified for this umbrella or legacy record; identify the exact product before searching.
      Source IDH51-950F78F7CBF3AB1CAFC97AC1

      No separate structured rows were bundled for preparation, IV push, continuous infusion, population dosing, dialysis, CRRT. Historical article content and source links may cover these topics.

      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 IDH51-1AB36D60FFA07017048E597B
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-ACF8EB5E16EDE434B8B0E551
      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-F3DDDEC4AFE007D7A6EDB00F

      Historical Warnings and safeguards

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

      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-BBF72EF76C2701FBE35B4913

      Historical Stability notes

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

      1. Legacy product stability information is not automatically equivalent to a USP <797> BUD.
        Source IDH51-205FD176461262AF3655F339
      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
      pentobarbital
      Source IDH51-2AC8BEFCD6D84AFC32655D4C
      Legacy title
      Pentobarbital
      Source IDH51-A5682EA8CB42492604EAAAB9
      Generic name
      Pentobarbital
      Source IDH51-22B512EC3A2C06AB80AD0166
      Class
      Sedation, analgesia, and anesthesia
      Source IDH51-BB479A6CCE66249E40271C61
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-1A2DF94216ADC42A49AA7064
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-3D4B0FA3527AC11BB0DE7547
      Populations
      1. Population not yet normalized
        Source IDH51-37E36E929BD364592030C694
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-738B30F58F4689A90DEEA422
      High alert
      false
      Source IDH51-6AE6D0FCE61ECC9556BE9998
      Hazardous
      false
      Source IDH51-97378AEBCA947B8E0ABA53F7
      Status
      Legacy migration
      Source IDH51-E53EA4BBD79A1C2FEA3CDE2A
      Version added
      Legacy
      Source IDH51-87B2126B98E34C5B1D3156DE
      Sources
      LabelUrlKind
      Source IDH51-5183EDEBBA81769B60617301
      GlobalRPh legacy IV dilution monograph
      Source IDH51-871CFFE15F1376B009A749D4
      legacy:auto
      Source IDH51-0677E6640C5C7662841D0856
      Legacy
      Source IDH51-1D2C23715C8552BB6EB3FB9D
      Clinical release verification
      Audit version
      3.4
      Source IDH51-56959F1FAC58BC937F85127F
      Audited on
      2026-08-30
      Source IDH51-920486EE39AB94F2256C99F4
      Level
      red
      Source IDH51-F87B40EB7C6C3C58579186CB
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-6F77ABADFA896BC31308BBE3
      Exact current label candidate
      false
      Source IDH51-2906A25D3FD9314A2955536B
      Reference url count
      0
      Source IDH51-403BFF2762D314D0192B0764
      Broken reference count
      0
      Source IDH51-7626BA8C46F5F9E61F19A76D
      Point of use confirmation required
      true
      Source IDH51-14E31792445B8C744509ABAF
      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-F2DD01759319F3411789F05A

      Dosing source fields

      Id
      pentobarbital
      Source IDH51-03E8366D2DA97D28D835EA2D
      Generic name
      Pentobarbital
      Source IDH51-74F0FBDF56E7E10B88470208
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-78529A2BAB91829D79264DB9
      Package insert
      Query name
      Pentobarbital
      Source IDH51-E1903CFEA697384404DC9938
      Product and route must match
      true
      Source IDH51-C063A595BE3FF2B3E74B1802
      Live current label enabled
      false
      Source IDH51-88C1A5DA09235ECB71DEAAF7
      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 IDH51-417BAD5932F0B647F4B72D48
      Direct official label access enabled
      true
      Source IDH51-E88C9A9F810A0FB80E73E1DE
      Outbound server request required
      false
      Source IDH51-4A2CFE84BF04E785967CBEF5
      Local summary status
      not_bundled
      Source IDH51-25DDFB77AD22F37533929C5C
      Clinical review
      Locally normalized
      false
      Source IDH51-2A094B12168E111044828AF0
      Reviewed
      2026-08-29
      Source IDH51-629DF31FA016FAD86E4011E6
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-84C712001F567BC49EBA7858
      Clinical release verification
      Audit version
      3.4
      Source IDH51-FB779A872B4EA53314B76BDE
      Audited on
      2026-08-30
      Source IDH51-1A95106FD0BB97C168056048
      Level
      red
      Source IDH51-697AC726D3ABBF4726A00D5B
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-550D987ABF321829C71802AF
      Exact current label candidate
      false
      Source IDH51-A2570973F40552D5961FF224
      Reference url count
      0
      Source IDH51-99F544F2257CFFFCE07624EE
      Broken reference count
      0
      Source IDH51-9BDA42B2F9BD34BCF07D8E37
      Point of use confirmation required
      true
      Source IDH51-FCBC19E5810C133102A12762
      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-EC0B1FA80DF62E54229B26B7
      Historical preparation assessment

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

      Id
      pentobarbital
      Source IDH51-A78413671745A79359121A48
      Name
      Pentobarbital
      Source IDH51-434B856F89652C1D7A7D294E
      Therapeutic class
      Sedation, analgesia, and anesthesia
      Source IDH51-50E591167C2771F904F32BDA
      Review version
      3.1
      Source IDH51-5CC1642C7274AFFA625F04C6
      Review date
      2026-08-30
      Source IDH51-89EC52916F3E850E07392542
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-B0B048BDC9D3071C034176E4
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-5A565FEF13E0E0924B854823
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-61A33D9EF99067F4C59C7463
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-53F9D00DD43C54B83FF4B572
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-261A539DFD9650DEA1A82732
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9EDF387B5EBAAF750D80939C
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-D6C62D43570CB80907C88F24
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-A60BD3E33824796702D117F0
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8DA556AD9CC9D28486A58622
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-B58413EAEF7B4A86D2C95D7C
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-38FDDCDF8E67D6302255968E
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-82F2D68C961ED4CE5EDCADF5
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-4A0807E60642880EBD96F596
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-8E7A339865A534D7B130BA6C
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-13F4FF828080A6DA62395938
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-252BA93E5A7AD78543797E9B
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-EF1D63794E0D6E8077E0670B
      Adult dosing range
      Primary
      not_found
      Source IDH51-0EE4555BF45C51FA61660EEA
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-6BAD6326899FA4BD7AD099E9
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-1EF847161A16542AF47D872E
      Infusion time
      Primary
      not_found
      Source IDH51-DC46FDA8649B376224FF8422
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-6CD8E2F209A64B6B670D7486
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-ECE5F92709B80AA1C71EAAAF
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-ECADDEB825775ADE58CAF4BB
      Guide generation allowed
      false
      Source IDH51-9BF5A32CB243A7217A5E9137
      Pediatric
      Applicability
      not_established
      Source IDH51-94B131F91BAAFF0AA9DF6F79
      Guide generation allowed
      false
      Source IDH51-8A1F7447012DF6B8D054D820
      Neonatal
      Applicability
      not_established
      Source IDH51-DC8E73F4F3032959B79622A5
      Guide generation allowed
      false
      Source IDH51-46EF87BB0B81D6970D8B43C3
      Route presence
      Structured dilution
      false
      Source IDH51-C2B247C540083E1EDBF88E2C
      Iv push
      false
      Source IDH51-2FBAB3EF068D61C842527C31
      Continuous infusion
      false
      Source IDH51-40A32C939431D6DA122A283D
      Pediatric source
      false
      Source IDH51-81A64E99D165658D28D98943
      Neonatal source
      false
      Source IDH51-56DB6E9FE00AFA03D49C1D51
      Legacy reference
      Status
      not_available
      Source IDH51-3A12BF05D9A777A0FBA6B95F
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-D8B61E0A7156C271ADF53F0D
      Source files
      1. catalog.json
        Source IDH51-F7C8217D534C672FE6B045ED
      2. dosing.json
        Source IDH51-CC8CD2E05619814E6AF2E495
      3. legacy-map.json
        Source IDH51-7E222BCD42602BA70EFAC756
      4. review-queue.json
        Source IDH51-AE3CACD0558C00C14C69CD06
      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 IDH51-4AFD5A8D0705664372BDD2CE
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-2AC8BEFCD6D84AFC32655D4Ccatalog.json
      /records/193/id
      Historical; current review incomplete
      H51-A5682EA8CB42492604EAAAB9catalog.json
      /records/193/legacy_title
      Historical; current review incomplete
      H51-22B512EC3A2C06AB80AD0166catalog.json
      /records/193/generic_name
      Historical; current review incomplete
      H51-BB479A6CCE66249E40271C61catalog.json
      /records/193/class
      Historical; current review incomplete
      H51-1A2DF94216ADC42A49AA7064catalog.json
      /records/193/subclass
      Historical; current review incomplete
      H51-3D4B0FA3527AC11BB0DE7547catalog.json
      /records/193/summary
      Historical; current review incomplete
      H51-BBF72EF76C2701FBE35B4913catalog.json
      /records/193/warnings/0
      Historical; current review incomplete
      H51-205FD176461262AF3655F339catalog.json
      /records/193/stability_notes/0
      Historical; current review incomplete
      H51-37E36E929BD364592030C694catalog.json
      /records/193/populations/0
      Historical; current review incomplete
      H51-738B30F58F4689A90DEEA422catalog.json
      /records/193/evidence_tier
      Historical; current review incomplete
      H51-6AE6D0FCE61ECC9556BE9998catalog.json
      /records/193/high_alert
      Historical; current review incomplete
      H51-97378AEBCA947B8E0ABA53F7catalog.json
      /records/193/hazardous
      Historical; current review incomplete
      H51-E53EA4BBD79A1C2FEA3CDE2Acatalog.json
      /records/193/status
      Historical; current review incomplete
      H51-F4F219BCFA36EC7D33DF2111catalog.json
      /records/193/reviewed
      Historical; current review incomplete
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