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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Methyldopate

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.

Methyldopate ( Aldomet ®) (opens in a new tab)Original source URL: https://globalrph.com/dilution/methyldopate-aldomet/ | 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/methyldopate-aldomet/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:48:26.494092+00:00
Source location
div.post-content
Packaged content SHA-256
813e12aa64fb94351a487fb25ce44377d59f434d80da4acc0089dab72826b1a9
Original response SHA-256
91362faf37712d824d13e315c928844764ffd43535263e08f6a0db39f7b32d28
Source body SHA-256
2bbbcdd3db08d6b1c20316fb4dbe095e73f58af3af718fb87fd0939026730df7

Methyldopate ( Aldomet ®)

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

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

[0 to 500 mg] [100 ml] [60 min]
[over 500 mg] [250 ml] [60 min]

Stability / Miscellaneous

EXP: 1 DAY (RT)

DOSAGE AND ADMINISTRATION
Methyldopate HCl Injection when given intravenously in effective doses, causes a decline in blood pressure that may begin in four to six hours and last 10 to 16 hours after injection.

Add the desired dose of Methyldopate HCl Injection to 100 mL of Dextrose Injection 5%, USP. Alternatively the desired dose may be given in 5% dextrose in water in a concentration of 100 mg/10 mL. Give this intravenous infusion slowly over a period of 30 to 60 minutes.

Adults: The usual adult dosage intravenously is 250 mg to 500 mg at six hour intervals as required. The maximum recommended intravenous dose is 1 gram every six hours.

When control has been obtained, oral therapy with tablets may be substituted for intravenous therapy, starting with the same dosage schedule used for the parenteral route. The effectiveness and anticipated responses are described in the circular for tablets.

Since methyldopate has a relatively short duration of action, withdrawal is followed by return of hypertension usually within 48 hours. This is not complicated by an overshoot of blood pressure.

Occasionally tolerance may occur, usually between the second and third month of therapy. Adding a diuretic or increasing the dosage of methyldopa frequently will restore effective control of blood pressure. A thiazide may be added at any time during methyldopa therapy and is recommended if therapy has not been started with a thiazide or if effective control of blood pressure cannot be maintained on 2 grams of methyldopa daily.

Methyldopa is largely excreted by the kidney and patients with impaired renal function may respond to smaller doses. Syncope in older patients may be related to an increased sensitivity and advanced arteriosclerotic vascular disease. This may be avoided by lower doses.

HOW SUPPLIED
Methyldopate HCl Injection, USP 250 mg/5 mL (50 mg/mL).
NDC 0517-8905-10 5 mL Single Dose Vial Boxes of 10

Store at controlled room temperature 15°-30°C (59°-86°F) (See USP).

Rx Only
IN8905
Rev. 12/02
MG #7604

American
Regent
Laboratories, Inc.
Shirley, NY 11967

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
      methyldopate
      Source IDH51-730F468E90E964C21FBE80CD
      Generic name
      Methyldopate
      Source IDH51-F1D88445CB888C7A6C966AA8
      Class
      Other intravenous medications
      Source IDH51-A11884D959C266D932EB856F
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-0537D4929FDDD20630146814
      Primary uses
      1. A specialized IV indication that requires confirmation in the current exact-product label and applicable specialty guidance.
        Source IDH51-5522CEDA1923435F2A322EA1
      Mechanism
      Is converted to alpha-methylnorepinephrine, a central alpha-2 agonist that reduces sympathetic outflow.
      Source IDH51-43759731FCA61E21C98898FF
      Mechanism level
      drug_specific
      Source IDH51-9290CF203F8D5B00629AF64E
      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 IDH51-0F8475E8DF76904A137E6CF2
      Administration orientation
      Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required.
      Source IDH51-77A964941A048BA4883392FE
      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 IDH51-6873FC4EC122748ACCAA7164
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-EC9BD8CFFF09053B082BC221
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-EB32D431FD22C7E7B7C5279B
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-61949560B20F933B302DBD26
      Legacy title
      Methyldopate
      Source IDH51-20582276493F697FC43D2C4D
      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 IDH51-1859732C4F53737ADABD0530
      Search text
      Methyldopate Other intravenous medications Legacy GlobalRPh directory entry A specialized IV indication that requires confirmation in the current exact-product label and applicable specialty guidance. Is converted to alpha-methylnorepinephrine, a central alpha-2 agonist that reduces sympathetic outflow. 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-B7D4902223E585E16074C63B
      Official access mode
      none
      Source IDH51-FB6AD8EEBBE830B361F27121
      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-F91C1BED0249209EDE09E85A

      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-F4168BC3532B8E3E3EAFDD43
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-C98A71D2389B909ECC077380
      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 IDH51-9B5AE7176954A860E71D34D9

      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 IDH51-51B5111EF91D8B4DC1CAD3B2

      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-CD2972DA6BEAE6A3A6602D5F
      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
      methyldopate
      Source IDH51-C61B35D25029C16B9898ED63
      Legacy title
      Methyldopate
      Source IDH51-92A113A9874FD12C09EFE148
      Generic name
      Methyldopate
      Source IDH51-2A8AC33D37EADC7BCD6F52AC
      Class
      Other intravenous medications
      Source IDH51-12C6D17398CE086A5DDEFD27
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-A8FA6CF000F244E313FFB90B
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-6870557156B2D685D7E915CF
      Populations
      1. Population not yet normalized
        Source IDH51-39DF96782DB56298BFA2A628
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-1C9608BB18D885C150721916
      High alert
      false
      Source IDH51-EEF1D9FB32E43142D450791C
      Hazardous
      false
      Source IDH51-47BB514AFC49CAC069BADB43
      Status
      Legacy migration
      Source IDH51-0DCDCFFDD655624AC4EB7C8A
      Version added
      Legacy
      Source IDH51-24C501C09C128D4AB6E1D2AD
      Sources
      LabelUrlKind
      Source IDH51-DAEF482F8D4C6847B5F5862E
      GlobalRPh legacy IV dilution monograph
      Source IDH51-E3AAB0CE5C476E5F574DD87F
      legacy:auto
      Source IDH51-EB504422FD2755A025446D42
      Legacy
      Source IDH51-171D834AC14770043EB37AAB
      Clinical release verification
      Audit version
      3.4
      Source IDH51-B2F6DDFFCD22D4DA43176868
      Audited on
      2026-08-30
      Source IDH51-C007B0AB097874510A8A7CC4
      Level
      red
      Source IDH51-F6C2D67E49BED6E4911E838A
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-4060468BAB1C018727A6390E
      Exact current label candidate
      false
      Source IDH51-9EAA1C335F837660E02FB2DB
      Reference url count
      0
      Source IDH51-BB334A644473D6770ECD2FA4
      Broken reference count
      0
      Source IDH51-DB95575473D5546945BAAD88
      Point of use confirmation required
      true
      Source IDH51-D328473C06879295E0C12250
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-8BB5484FCDCFB2E7495FC47B

      Dosing source fields

      Id
      methyldopate
      Source IDH51-543289438791B36F102ECBEA
      Generic name
      Methyldopate
      Source IDH51-5A18A8C76967D5E40E075F71
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-34454677382FF9A75C304B67
      Package insert
      Query name
      Methyldopate
      Source IDH51-703DDA726FBE68B2346231C6
      Product and route must match
      true
      Source IDH51-EBE0EB8DD744AF5B5A63D461
      Live current label enabled
      false
      Source IDH51-03970CA24BCF41F5A708D066
      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-DCA0A2B7EECAAB2FAC2A21CB
      Direct official label access enabled
      true
      Source IDH51-3CA6F5085663BD5C9203AF4D
      Outbound server request required
      false
      Source IDH51-DE479C093E695A2611DC06F4
      Local summary status
      not_bundled
      Source IDH51-1C03F5BFD67AB63514C0061A
      Clinical review
      Locally normalized
      false
      Source IDH51-7290D477CF255535460B4347
      Reviewed
      2026-08-29
      Source IDH51-D85F64926E5E7C2B9BDBE3D9
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-F8AF1C300ACAC19F022AB65C
      Clinical release verification
      Audit version
      3.4
      Source IDH51-ADF4F681A47FA10558369B71
      Audited on
      2026-08-30
      Source IDH51-A8CF1397C282100F37DD3668
      Level
      red
      Source IDH51-8409C143A735FC3231DAD322
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-73C8655EEBC92749F2BA25CD
      Exact current label candidate
      false
      Source IDH51-3A15AA86C23195BD45F1E928
      Reference url count
      0
      Source IDH51-D75502812A6C286DF2F12BC8
      Broken reference count
      0
      Source IDH51-05A2E176391FCB175039ED97
      Point of use confirmation required
      true
      Source IDH51-0AE8E7373E09B024576961BF
      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-EF6374528D69AF4C91A13405
      Historical preparation assessment

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

      Id
      methyldopate
      Source IDH51-3D3F3D57EA9900A668EB1244
      Name
      Methyldopate
      Source IDH51-AAAB03FDFB296CC66447690E
      Therapeutic class
      Other intravenous medications
      Source IDH51-DB6CC7C3B0468AD37296DF97
      Review version
      3.1
      Source IDH51-B7ECFF0E7EAF5E77726FB400
      Review date
      2026-08-30
      Source IDH51-59F6F25E9304E9614727A963
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-9B2F44A8D37345181B940FC0
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-DD106E013185F790A6C2D0A7
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-6BA0DDC9912045C65963D8EF
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-A1A5B7E01A995A7D945FE279
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-6611F6E69FF5EEB866816E7F
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9FD2AD903232D089ACD76502
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-12D3DCEC8C8B88D4705C4F45
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-FCE4DC838007CD8DC05DAED5
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-7AC122FA7C59B5E4155663D6
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-08A619A5484766D799AB0020
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-1CBB45269A2F7E228AB6168D
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-A00AE9D19A7178CEE0E382F2
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-1F2C377A5D902D4F6651D9BF
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-9983A0534CA980610CE46A78
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-296B733E8DF7540FF7F2E175
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-9386C8CCEF524C4CD4F1A047
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-317EF84A314F497B650D0A16
      Adult dosing range
      Primary
      not_found
      Source IDH51-BC7FDE570FAA4F13FAF7069C
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-95D08E09B3229D0C1C5FBB75
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-526AD33A1A990DB1418FEDB3
      Infusion time
      Primary
      not_found
      Source IDH51-37EF8E84ACB92A6B5AA362D9
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-712C6A39E0D56CE981DBA095
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-35501767652A2B7CE7F61327
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-D373A3D3EB7CCFF7BB25252C
      Guide generation allowed
      false
      Source IDH51-6893226C8E096EB48BC44D42
      Pediatric
      Applicability
      not_established
      Source IDH51-EF57071A832D483E11716B58
      Guide generation allowed
      false
      Source IDH51-3AC695377E9F04E088426CC4
      Neonatal
      Applicability
      not_established
      Source IDH51-BE46CED045EF5ADE4C6F98B2
      Guide generation allowed
      false
      Source IDH51-DB99074F7314DDCA208C4251
      Route presence
      Structured dilution
      false
      Source IDH51-EF91EBD5061CF02CF3230752
      Iv push
      false
      Source IDH51-90C2997E64718AE4DB8E0B15
      Continuous infusion
      false
      Source IDH51-DD331FAFE003374CFC5EBF93
      Pediatric source
      false
      Source IDH51-4C00E1F6989F165690F44800
      Neonatal source
      false
      Source IDH51-36F8F0C489D6E7201F856EDC
      Legacy reference
      Status
      not_available
      Source IDH51-98059E41404ADFF8F65A549D
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-8CA9FBE9EC35E59F12336D8D
      Source files
      1. catalog.json
        Source IDH51-F32F27884D1F7FD44668CE81
      2. dosing.json
        Source IDH51-890B22A1D71355AEB519EA65
      3. legacy-map.json
        Source IDH51-93E483296E03D93AF04ED495
      4. review-queue.json
        Source IDH51-A5A309E82665D119A2054A00
      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 IDH51-95E34F78E16C2930CF334886
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-C61B35D25029C16B9898ED63catalog.json
      /records/160/id
      Historical; current review incomplete
      H51-92A113A9874FD12C09EFE148catalog.json
      /records/160/legacy_title
      Historical; current review incomplete
      H51-2A8AC33D37EADC7BCD6F52ACcatalog.json
      /records/160/generic_name
      Historical; current review incomplete
      H51-12C6D17398CE086A5DDEFD27catalog.json
      /records/160/class
      Historical; current review incomplete
      H51-A8FA6CF000F244E313FFB90Bcatalog.json
      /records/160/subclass
      Historical; current review incomplete
      H51-6870557156B2D685D7E915CFcatalog.json
      /records/160/summary
      Historical; current review incomplete
      H51-51B5111EF91D8B4DC1CAD3B2catalog.json
      /records/160/warnings/0
      Historical; current review incomplete
      H51-CD2972DA6BEAE6A3A6602D5Fcatalog.json
      /records/160/stability_notes/0
      Historical; current review incomplete
      H51-39DF96782DB56298BFA2A628catalog.json
      /records/160/populations/0
      Historical; current review incomplete
      H51-1C9608BB18D885C150721916catalog.json
      /records/160/evidence_tier
      Historical; current review incomplete
      H51-EEF1D9FB32E43142D450791Ccatalog.json
      /records/160/high_alert
      Historical; current review incomplete
      H51-47BB514AFC49CAC069BADB43catalog.json
      /records/160/hazardous
      Historical; current review incomplete
      H51-0DCDCFFDD655624AC4EB7C8Acatalog.json
      /records/160/status
      Historical; current review incomplete
      H51-F4543FE61B9F210BA9BC99BBcatalog.json
      /records/160/reviewed
      Historical; current review incomplete
      H51-24C501C09C128D4AB6E1D2ADcatalog.json
      /records/160/version_added
      Historical; current review incomplete
      H51-DAEF482F8D4C6847B5F5862Ecatalog.json
      /records/160/sources/0
      Historical; current review incomplete
      H51-E3AAB0CE5C476E5F574DD87Fcatalog.json
      /records/160/sources/0/label
      Historical; current review incomplete
      H51-EB504422FD2755A025446D42catalog.json
      /records/160/sources/0/url
      Historical; current review incomplete
      H51-171D834AC14770043EB37AABcatalog.json
      /records/160/sources/0/kind
      Historical; current review incomplete
      H51-B2F6DDFFCD22D4DA43176868catalog.json
      /records/160/clinical_release_verification/audit_version
      Historical; current review incomplete
      H51-C007B0AB097874510A8A7CC4catalog.json
      /records/160/clinical_release_verification/audited_on
      Historical; current review incomplete
      H51-F6C2D67E49BED6E4911E838Acatalog.json
      /records/160/clinical_release_verification/level
      Historical; current review incomplete
      H51-4060468BAB1C018727A6390Ecatalog.json
      /records/160/clinical_release_verification/release_gate
      Historical; current review incomplete
      H51-9EAA1C335F837660E02FB2DBcatalog.json
      /records/160/clinical_release_verification/exact_current_label_candidate
      Historical; current review incomplete
      H51-D3664DB475601587C8517B48catalog.json
      /records/160/clinical_release_verification/selected_setid
      Historical; current review incomplete
      H51-8E690F79C395E09D7D08100Bcatalog.json
      /records/160/clinical_release_verification/selected_label_title
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