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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Prochlorperazine

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.

Prochloroperazine - Compazine ® (opens in a new tab)Original source URL: https://globalrph.com/dilution/prochloroperazine-compazine/ | 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/prochloroperazine-compazine/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:47:21.319626+00:00
Source location
div.post-content
Packaged content SHA-256
839712fa064eb84284d139d92513f447a5a427fb57b30fd052c6b0fe11042336
Original response SHA-256
b1763776fb0f028c145834df6322f63c8d52d108b0fe52e5fd3e01fa89ca4cf4
Source body SHA-256
1155899d3dca410cf6bc1e79b134707ee17b5d840ee8e46a7bc9ead8eb036676

Prochlorperazine Edisylate (Compazine ® )

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]

[0 to 20mg] [50 ml] [30 min]

I.V. Dosage
5 to 10 mg (1 to 2 mL) as a slow I.V. injection or infusion 15 to 30 minutes before induction of anesthesia, or to control acute symptoms during or after surgery. Repeat once if necessary.

Compazine (prochlorperazine) may be administered either undiluted or diluted in isotonic solution, but a single dose of the drug should not exceed 10 mg. The rate of administration should not exceed 5 mg per minute. When administered I.V., do not use bolus injection.

Stability / Miscellaneous

Label: Protect from light.

Single doses normally should not exceed 10mg.
Maximum rate (IV-push): 5 mg/min (usual: 2.5 mg/min).
Usual rate (infusion): 1 mg/min.
Maximum recommended dose/day: 40 mg.
Some studies have used high dose compazine (30-40mg) over 20-30 minutes prior to chemotherapy.

DOSAGE AND ADMINISTRATION
Notes on Injection
Stability-This solution should be protected from light. This is a clear, colorless to pale yellow solution; a slight yellowish discoloration will not alter potency. If markedly discolored, solution should be discarded.

Compatibility-It is recommended that Compazine (prochlorperazine) Injection not be mixed with other agents in the syringe.

DOSAGE AND ADMINISTRATION-ADULTS
Dosage should be increased more gradually in debilitated or emaciated patients.

Elderly Patients
In general, dosages in the lower range are sufficient for most elderly patients. Since they appear to be more susceptible to hypotension and neuromuscular reactions, such patients should be observed closely. Dosage should be tailored to the individual, response carefully monitored and dosage adjusted accordingly. Dosage should be increased more gradually in elderly patients.

1. To Control Severe Nausea and Vomiting
Adjust dosage to the response of the individual. Begin with the lowest recommended dosage.

I.M. Dosage
Initially 5 to 10 mg (1 to 2 mL) injected deeply into the upper outer quadrant of the buttock. If necessary, repeat every 3 or 4 hours. Total I.M. dosage should not exceed 40 mg per day.

I.V. Dosage
2.5 to 10 mg (0.5 to 2 mL) by slow I.V. injection or infusion at a rate not to exceed 5 mg per minute. Compazine Injection may be administered either undiluted or diluted in isotonic solution. A single dose of the drug should not exceed 10 mg; total I.V. dosage should not exceed 40 mg per day. When administered I.V., do not use bolus injection. Hypotension is a possibility if the drug is given by I.V. injection or infusion.

Subcutaneous administration is not advisable because of local irritation.

2. Adult Surgery (for severe nausea and vomiting)
Total parenteral dosage should not exceed 40 mg per day. Hypotension is a possibility if the drug is given by I.V. injection or infusion.

I.M. Dosage
5 to 10 mg (1 to 2 mL) 1 to 2 hours before induction of anesthesia (repeat once in 30 minutes, if necessary), or to control acute symptoms during and after surgery (repeat once if necessary).

I.V. Dosage
5 to 10 mg (1 to 2 mL) as a slow I.V. injection or infusion 15 to 30 minutes before induction of anesthesia, or to control acute symptoms during or after surgery. Repeat once if necessary. Compazine (prochlorperazine) may be administered either undiluted or diluted in isotonic solution, but a single dose of the drug should not exceed 10 mg. The rate of administration should not exceed 5 mg per minute. When administered I.V., do not use bolus injection.

3. In Adult Psychiatric Disorders
Adjust dosage to the response of the individual and according to the severity of the condition. Begin with the lowest recommended dose. Although response ordinarily is seen within a day or 2, longer treatment is usually required before maximal improvement is seen.

I.M. Dosage
For immediate control of adult schizophrenic patients with severe symptomatology, inject an initial dose of 10 to 20 mg (2 to 4 mL) deeply into the upper outer quadrant of the buttock. Many patients respond shortly after the first injection. If necessary, however, repeat the initial dose every 2 to 4 hours (or, in resistant cases, every hour) to gain control of the patient. More than three or four doses are seldom necessary. After control is achieved, switch patient to an oral form of the drug at the same dosage level or higher. If, in rare cases, parenteral therapy is needed for a prolonged period, give 10 to 20 mg (2 to 4 mL) every 4 to 6 hours. Pain and irritation at the site of injection have seldom occurred.

Subcutaneous administration is not advisable because of local irritation.

HOW SUPPLIED
Vials
2 mL (5 mg/mL), in boxes of 25 and 10 mL (5 mg/mL), in boxes of 1.

2 mL (5 mg/mL), in boxes of 25: NDC 0007-3352-16

10 mL (5 mg/mL), in boxes of 1: NDC 0007-3343-01

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
      prochlorperazine
      Source IDH51-CC114CBB277A0B5CE45FD121
      Generic name
      Prochlorperazine
      Source IDH51-70B80DCD2A11E5BEA74D2127
      Class
      GI and antiemetic
      Source IDH51-12DAB79FF9BECE8072B31991
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-F07E3B6211EEB5C540D2FAE5
      Primary uses
      1. Acid suppression, nausea and vomiting control, or gastrointestinal motility therapy, depending on the named agent.
        Source IDH51-B3912094F3A0A1BFE809E4FB
      Mechanism
      Blocks central dopamine D2 receptors; additional receptor effects vary by agent.
      Source IDH51-7427841806A5D1409A9E66CD
      Mechanism level
      drug_specific
      Source IDH51-0180200D8390429963A4A026
      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 IDH51-1BA1ECC10BE83C2C2D1FC34D
      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-FC61DBEE236D69BC8FC41D86
      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 IDH51-52276DA6DFDB9145F2161150
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-34D61EA3BC1341692BCB6FAB
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-0E1D6C7DA6C31AB41C374E80
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-5698CEE41DF573DCAFA8D098
      Legacy title
      Prochlorperazine
      Source IDH51-460DC4E2D7D47AA71BAAACFA
      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-FE5FCEDB87ED6A4DC7D67A7B
      Search text
      Prochlorperazine GI and antiemetic Legacy GlobalRPh directory entry Acid suppression, nausea and vomiting control, or gastrointestinal motility therapy, depending on the named agent. Blocks central dopamine D2 receptors; additional receptor effects vary by agent. 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 IDH51-4E060B3B5ABF3D8653BBB7E8
      Official access mode
      none
      Source IDH51-33061FCA4A3EF8211C189601
      Official access reason
      No source-backed DailyMed action has been verified for this umbrella or legacy record; identify the exact product before searching.
      Source IDH51-040603FA86F8B27D28E46799

      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 IDH51-0EF60B016DC58FB19ACC6782
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-AA76088F16F8AFB8D03135EB
      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 IDH51-3947CFF8AC3E4745A9EA2529

      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 IDH51-54BF613DA704F46CC5BDB768

      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-E1FB62AE718CB4AF94E0971E
      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
      prochlorperazine
      Source IDH51-1A74C334752C157A60BBFFE8
      Legacy title
      Prochlorperazine
      Source IDH51-4CDF6AF1FCE8438E2A819521
      Generic name
      Prochlorperazine
      Source IDH51-92DF471C3DC0C1B9C592B7CF
      Class
      GI and antiemetic
      Source IDH51-39F3FAB020A46CE4E3172771
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-239DA9FD6C5B1FE182254B65
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-82D95CF26FF17FE84CB569D4
      Populations
      1. Population not yet normalized
        Source IDH51-D997C288B77403FE2411056F
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-0B566581514859A7BB1D0D1D
      High alert
      false
      Source IDH51-0033D8260722D3A6AD5C5580
      Hazardous
      false
      Source IDH51-F16BF90D5D68A91EAFC78FBB
      Status
      Legacy migration
      Source IDH51-79248130F9F49977265FDC38
      Version added
      Legacy
      Source IDH51-91101370CAD614B034333CEF
      Sources
      LabelUrlKind
      Source IDH51-FACD83427C6D2B9BC0308DE9
      GlobalRPh legacy IV dilution monograph
      Source IDH51-C99E0A53D8A794A033EA6997
      legacy:auto
      Source IDH51-D60C60A6CFB8F453758449FA
      Legacy
      Source IDH51-B79E47AD2DD3FAF61D0CAF25
      Clinical release verification
      Audit version
      3.4
      Source IDH51-C03168F38B86275A619F54B0
      Audited on
      2026-08-30
      Source IDH51-A5D1F4D33E5231A7CEC227EC
      Level
      red
      Source IDH51-C2DAC2A4F889B122F3C03611
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-D176DA73EE8B9DA9DE2A9015
      Exact current label candidate
      false
      Source IDH51-08F201F7251B735E5ADB4C9E
      Reference url count
      0
      Source IDH51-9FE6BBD0C2177938D07098F5
      Broken reference count
      0
      Source IDH51-E2F0A119CFDA772FB0E411B1
      Point of use confirmation required
      true
      Source IDH51-4B8BC830E16A009A55ABB333
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-6C6E94EE2EA1A84C733467E7

      Dosing source fields

      Id
      prochlorperazine
      Source IDH51-63730D238203516319FE5C71
      Generic name
      Prochlorperazine
      Source IDH51-48537138ECC6568FE969C8C4
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-76D1009EE9E61DABBAC9D04C
      Package insert
      Query name
      Prochlorperazine
      Source IDH51-C6DA13B51B7739A73CF39979
      Product and route must match
      true
      Source IDH51-58B9AFEC87B8A32C3BDCCEBB
      Live current label enabled
      false
      Source IDH51-2540703E1ECE9E9883C92D07
      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 IDH51-7F7A14F3173818D7AE8F2419
      Direct official label access enabled
      true
      Source IDH51-881C74FCBA606647CF3EEAC3
      Outbound server request required
      false
      Source IDH51-5B3F3A30D1B2531F1DCFA833
      Local summary status
      not_bundled
      Source IDH51-5D1B8767E89D23ED92B43EF1
      Clinical review
      Locally normalized
      false
      Source IDH51-AA586587B9BA68504FF167A7
      Reviewed
      2026-08-29
      Source IDH51-617971D31DA5CDD2C4B7D5EE
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-A48325EA3FC5114A1441A592
      Clinical release verification
      Audit version
      3.4
      Source IDH51-DC279EB0E0C3D96DF379B590
      Audited on
      2026-08-30
      Source IDH51-01ED67045196B1DD07FDAD08
      Level
      red
      Source IDH51-54DE8F8A8BD8E7C1B84FEB0C
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-B3664CA96B6AA72F4F4D7E06
      Exact current label candidate
      false
      Source IDH51-D845F11F7B3A265B131CD5D6
      Reference url count
      0
      Source IDH51-D11E2A73C927C68C7918D672
      Broken reference count
      0
      Source IDH51-2036F8C3E08BCE8035CA8992
      Point of use confirmation required
      true
      Source IDH51-0C1F03F5A73189398028BB28
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-2CF7B00B10074BAACB024B4D
      Historical preparation assessment

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

      Id
      prochlorperazine
      Source IDH51-5F59F94486A7DBC6237384C2
      Name
      Prochlorperazine
      Source IDH51-0A4F5FDA764056F9540CB33C
      Therapeutic class
      GI and antiemetic
      Source IDH51-6F38266E7A87AD91F2505657
      Review version
      3.1
      Source IDH51-1924CF1EBA2AD24F57BD08A9
      Review date
      2026-08-30
      Source IDH51-A8AAAB370C51CE4642ACBBC9
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-8D84D1A394816923E870E72E
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-003AAC35B868D8A54C6C8822
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-013DF0E11BA2C0DAC0C0998F
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-88F39D3FDCFD563F52EF5969
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-23DB7F16EEF7FD019D713D7B
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-6AA5B1F21728A606CFAF05FF
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-7A442FBB261A37B0DF1A46C5
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-150B2957DD1EAE8CE6CBBEAA
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8A538849B4CDF2D36B3B4EEF
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-D0F99E614C2206766F4C5536
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-EE7B100F2C21344E3DFAF15B
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-180EE20B8260D78F67B57B50
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-11D5F46D7ED6F2C63FA695F6
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-B64653ADC8A8536B86BECF93
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-D10106FFB3AA86E3602BB324
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-E80A37AFA3B10AA7DA166089
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-CE6CD4BC57A19C1B3B6AFE13
      Adult dosing range
      Primary
      not_found
      Source IDH51-CE6D403BFFC7941D98A2096D
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-DEB2AFD749F2814FFEC27933
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-311A5D99FDA7ECC108991E38
      Infusion time
      Primary
      not_found
      Source IDH51-E829685729F989F9EC368D06
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-3436AF390C73E5F83CC3A7AE
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-59DC91FF4BED5DF98E1E6FBE
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-67E6BCB664973AD295E49591
      Guide generation allowed
      false
      Source IDH51-7B4476145004A3C151C31884
      Pediatric
      Applicability
      not_established
      Source IDH51-FF342CBB3D0F33D04988B781
      Guide generation allowed
      false
      Source IDH51-6A907B2E327C8B6E6EEF1A3C
      Neonatal
      Applicability
      not_established
      Source IDH51-3258FD6EDD9C1A568D63113F
      Guide generation allowed
      false
      Source IDH51-FB8F7F7F390E74DE412D958C
      Route presence
      Structured dilution
      false
      Source IDH51-3C0975F2A82512A596F29DD5
      Iv push
      false
      Source IDH51-864EEA12AF8758F10F410D84
      Continuous infusion
      false
      Source IDH51-0D15E0B84AFE4DF03F42134B
      Pediatric source
      false
      Source IDH51-F405C162F27954B3A1138C1B
      Neonatal source
      false
      Source IDH51-82AE8EC5816DAFBDEE46E2E6
      Legacy reference
      Status
      not_available
      Source IDH51-FB634C6F5141A111715E5353
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-0FEAB925FB238F634641AE6F
      Source files
      1. catalog.json
        Source IDH51-8923BD5C09DE06176CCB3845
      2. dosing.json
        Source IDH51-DCF6C8440E44389CF0FB9FC0
      3. legacy-map.json
        Source IDH51-88AF41C62FDA4DF6A4BD50B6
      4. review-queue.json
        Source IDH51-3D6A44498B8E8DCE012DD55C
      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-AD8F248C7D7C1205E79427FC
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-1A74C334752C157A60BBFFE8catalog.json
      /records/206/id
      Historical; current review incomplete
      H51-4CDF6AF1FCE8438E2A819521catalog.json
      /records/206/legacy_title
      Historical; current review incomplete
      H51-92DF471C3DC0C1B9C592B7CFcatalog.json
      /records/206/generic_name
      Historical; current review incomplete
      H51-39F3FAB020A46CE4E3172771catalog.json
      /records/206/class
      Historical; current review incomplete
      H51-239DA9FD6C5B1FE182254B65catalog.json
      /records/206/subclass
      Historical; current review incomplete
      H51-82D95CF26FF17FE84CB569D4catalog.json
      /records/206/summary
      Historical; current review incomplete
      H51-54BF613DA704F46CC5BDB768catalog.json
      /records/206/warnings/0
      Historical; current review incomplete
      H51-E1FB62AE718CB4AF94E0971Ecatalog.json
      /records/206/stability_notes/0
      Historical; current review incomplete
      H51-D997C288B77403FE2411056Fcatalog.json
      /records/206/populations/0
      Historical; current review incomplete
      H51-0B566581514859A7BB1D0D1Dcatalog.json
      /records/206/evidence_tier
      Historical; current review incomplete
      H51-0033D8260722D3A6AD5C5580catalog.json
      /records/206/high_alert
      Historical; current review incomplete
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