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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Multivitamin injection

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.

Multivitamin (MVI) (opens in a new tab)Original source URL: https://globalrph.com/dilution/multivitamin-mvi/ | 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/multivitamin-mvi/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:48:52.082558+00:00
Source location
div.post-content
Packaged content SHA-256
7f3782d0a2c6f89196a2847b10b7da7255fcffa928caeb3762fc484a2a44c8f6
Original response SHA-256
980a9e993438ab7ca058b6a9b581dc376687ef09e6ed498a7cd0b7a42530b7d5
Source body SHA-256
4257cb44643acda070db2ef2ef922215fcb4eedb26972b55660610e0894fa21e

MVI (Multiple Vitamins for Infusion) - INFUVITE ® ADULT

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, similar infusion solutions.

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

[Vial-1 (5ml) + Vial-2 (5ml) -10ml total ] [500 - 1000 ml ] [Range: 40 to 500 ml/hr]
Note: 1000 ml is the preferred infusion volume.

Label: Refrigerate.

Infusion rate: Maximum infusion rate not listed. Based on the possiblitity of an infusion related adverse reaction [e.g. urticaria, shortness of breath, wheezing and angioedema.] the maximum rate should probably not exceed 500 ml/hr (or 250 ml/hr max if a 500ml bag is used). [slower infusions reduce overall exposure and allow for prompt corrective action if an adverse effect is observed]

Allergic reactions have been known to occur following intravenous administration of thiamine, and vitamin K. The formulation is contraindicated prior to blood sampling for detection of megaloblastic anemia, as the folic acid and the cyanocobalamin in the vitamin solution can mask serum deficits.

Stability / Miscellaneous

WARNINGS: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solution, which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates who receive parenteral levels of aluminum at greater than 4 to 5 µg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.

Caution should be exercised when administering INFUVITE ADULT ® to patients on warfarin sodium-type anticoagulant therapy. In such patients, vitamin K may antagonize the hypothrombinemic response to anticoagulant drugs, such as warfarin and its congeners. Therefore, periodic monitoring of prothrombin/INR response is essential in determining the appropriate dosage of anticoagulant therapy.

INFUVITE ADULT - Multiple Vitamins for Infusion

Each 5 mL of Vial 1* contains:
Ascorbic acid (Vitamin C).........................................................200 mg
Vitamin A** (as palmitate)......................................................3 300 IU
Vitamin D3** (cholecalciferol)....................................................200 IU
Thiamine (Vitamin B1) (as the hydrochloride)...............................6 mg
Riboflavin (Vitamin B2) (as riboflavin 5-phosphate sodium).............3.6 mg
Pyridoxine HCl (Vitamin B6)........................................................6 mg
Niacinamide..........................................................................40 mg
Dexpanthenol (as d-pantothenyl alcohol)....................................15 mg
Vitamin E** (dl-a-tocopheryl acetate)..........................................10 IU
Vitamin K**............................................................................150 mcg
* with 1.4 % polysorbate 80, sodium hydroxide and/or hydrochloric acid for pH
adjustment and water for injection. ** Polysorbate 80 is used to water solubilize the oil-soluble vitamins A, D, E and K.
Each 5 mL of Vial 2† contains:
Folic acid...................................................................... 600 mcg
Biotin...............................................................................60 mcg
Vitamin B12 (cyanocobalamin)........................................5 mcg

† with 30 % propylene glycol, citric acid and/or sodium citrate for pH adjustment and water for injection.

DOSAGE AND ADMINISTRATION:
INFUVITE ADULT is ready for immediate use in adults and children aged 11 years and older when added to intravenous infusion fluids. INFUVITE ADULT should not be given as a direct, undiluted intravenous injection as it may give rise to dizziness, faintness and possible tissue irritation.
Preparation of INFUVITE ADULT for intravenous feeding should be done by transferring the contents of Vial 1 into the contents of Vial 2 (10 mL total). One daily 10 mL dose should be added directly to not less than 500 mL, and preferably 1 000 mL, of intravenous dextrose, saline or similar infusion solutions. Discard any unused portion.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
After INFUVITE ADULT is diluted in an intravenous infusion, the resulting solution should be refrigerated unless it is to be used immediately. The solution should be used within 24 hours after dilution. Some of the vitamins in this product, particularly A, D and riboflavin, are light sensitive; therefore, exposure to light should be minimized. Once closure system has been compromised, withdrawal of container contents should be completed within 4 hours.

Store under refrigeration, 2-8 °C (36-46 °F).

Reference:
Multiple Vitamins for Infusion - INFUVITE® [package insert]. Boucherville, QC, Canada: Sab-Pharma Inc., May 21, 2003

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
      multivitamin-injection
      Source IDH51-065BAC45EF6225659E41E88E
      Generic name
      Multivitamin injection
      Source IDH51-90048560A53DB439DECDB62D
      Class
      Electrolytes and fluids
      Source IDH51-7B1B989DA44E5DA208F59CC4
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-18F170ED012BD535044E6787
      Primary uses
      1. Correction of the named fluid, electrolyte, acid-base, or oncotic abnormality under monitored conditions.
        Source IDH51-406B5CF62C21D617E0D1E1D0
      Mechanism
      Replaces water- and fat-soluble vitamins that serve as metabolic cofactors and substrates.
      Source IDH51-DEB6ABDD3657C7D543A1E1FF
      Mechanism level
      drug_specific
      Source IDH51-720D6E7EB4E379737F2E79DF
      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 IDH51-5D085DAC8CAC2D32F6274F78
      Administration orientation
      Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required.
      Source IDH51-480B3DB99F949638E7E28E60
      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 IDH51-19F47C35888279C461B0F0FB
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-9E9FBD21DB71D18DB57AAAF3
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-AD122811B7523928F8AEC1D5
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-D71384A43905090F39C10B14
      Legacy title
      Multivitamin injection
      Source IDH51-12D3EB27C006E81B22CAAFED
      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-D5642C9C8AFB30CF25A76C0E
      Search text
      Multivitamin injection Electrolytes and fluids Legacy GlobalRPh directory entry Correction of the named fluid, electrolyte, acid-base, or oncotic abnormality under monitored conditions. Replaces water- and fat-soluble vitamins that serve as metabolic cofactors and substrates. 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 IDH51-663D8036F36E91F7B749F148
      Official access mode
      none
      Source IDH51-23F816CD6D3DF76BD72DC2EF
      Official access reason
      No source-backed DailyMed action has been verified for this umbrella or legacy record; identify the exact product before searching.
      Source IDH51-354B0C3C1D0223249942696C

      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-CA82F45484C10BCC2F122780
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-3B5982E04B3CB4041421D48C
      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 IDH51-92C890587D85526DA8E9DFCE

      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 IDH51-9F413ECBDC3292A961EB4579

      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 IDH51-40F6C8934E61D257828A97BD
      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
      multivitamin-injection
      Source IDH51-AAA1635A4D74D1759C6A2A17
      Legacy title
      Multivitamin injection
      Source IDH51-0F18F7CFD2D9C2F8C3BE6406
      Generic name
      Multivitamin injection
      Source IDH51-0BB5F09BD7A8FCFF313C2002
      Class
      Electrolytes and fluids
      Source IDH51-0BFE5DCC04C64C0F5F9686CD
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-07A3E03DD4F14DAB0394AAFE
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-4CFCB80661D6AAF7870C291D
      Populations
      1. Population not yet normalized
        Source IDH51-3C6106FD52B083887C42FD3D
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-E1CEDA903A875555C94DB3B7
      High alert
      false
      Source IDH51-DD09356855525823248B9FD5
      Hazardous
      false
      Source IDH51-88BFEBC9751ECB95048EFD17
      Status
      Legacy migration
      Source IDH51-044DC44931A1B5AF444E891D
      Version added
      Legacy
      Source IDH51-DEAB185FCE00DEB8BB01274F
      Sources
      LabelUrlKind
      Source IDH51-8CC2E51B77EC211C2BFBDC5E
      GlobalRPh legacy IV dilution monograph
      Source IDH51-335D17E64FE8285BBAE3C5D2
      legacy:auto
      Source IDH51-D95E34E702B377ACF4CF6EF5
      Legacy
      Source IDH51-990FC722EE9EA4DD9A5295B7
      Clinical release verification
      Audit version
      3.4
      Source IDH51-5C73C06BA2531547F2FBAF40
      Audited on
      2026-08-30
      Source IDH51-4DA7F319C228BCD3DF7377DD
      Level
      red
      Source IDH51-FE5A1C88FE355024C7E597CF
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-3A9E385F4A3651EC1ED3729D
      Exact current label candidate
      false
      Source IDH51-5A37B5E7CA2E2E1C3B42980B
      Reference url count
      0
      Source IDH51-AD166033AA8EF35C981F9BF0
      Broken reference count
      0
      Source IDH51-8435380A30267EAB2C70B220
      Point of use confirmation required
      true
      Source IDH51-6313D8ADE8270609FFBED98D
      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-DE9AE07AA65BECF7DC7364E6

      Dosing source fields

      Id
      multivitamin-injection
      Source IDH51-DB3FC5FFB344A0B2A83C15A7
      Generic name
      Multivitamin injection
      Source IDH51-EF558A7F4A6316E1D234BD71
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-1F4F2C3C2970C405CC65953F
      Package insert
      Query name
      Multivitamin injection
      Source IDH51-B111F6C928513006CDBED999
      Product and route must match
      true
      Source IDH51-6701339B7FAE5AE9B247751C
      Live current label enabled
      false
      Source IDH51-673897E78B0D165C878AD1A7
      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 IDH51-9714873F4E34E23C99351BD7
      Direct official label access enabled
      true
      Source IDH51-40E7216995FCCC50E0E60E53
      Outbound server request required
      false
      Source IDH51-5BF41A1F1A98A4EE3332B265
      Local summary status
      not_bundled
      Source IDH51-EE635CDB124D22243E9B9173
      Clinical review
      Locally normalized
      false
      Source IDH51-46CB1ADA2A09DAB9EBD3E9DD
      Reviewed
      2026-08-29
      Source IDH51-D63CAC8FB61B705471686CC1
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-99034268F00FC184F55B4558
      Clinical release verification
      Audit version
      3.4
      Source IDH51-F87A808C249CC45CCC42B5BB
      Audited on
      2026-08-30
      Source IDH51-ED41D7C2920DD7D52A4C85D4
      Level
      red
      Source IDH51-C8D69E7031D025B054DB2087
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-0612CB08D99B6F684598E51F
      Exact current label candidate
      false
      Source IDH51-46AAB4B9BEA5D0591F0E2A40
      Reference url count
      0
      Source IDH51-3DCD86EB44EB9CFE4E30964A
      Broken reference count
      0
      Source IDH51-2DB1CCB02B0EA42D24CA5B58
      Point of use confirmation required
      true
      Source IDH51-8E5AC8F396C8E7A145A751D6
      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-CC591C673CDB5258BCA70E21
      Historical preparation assessment

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

      Id
      multivitamin-injection
      Source IDH51-4C39079B729B38FF6D261C9F
      Name
      Multivitamin injection
      Source IDH51-8E438C706D37B529FE3CCDD6
      Therapeutic class
      Electrolytes and fluids
      Source IDH51-6038E140969D1AFE99579C5F
      Review version
      3.1
      Source IDH51-3C6EDDB8F8F0A78814363A9A
      Review date
      2026-08-30
      Source IDH51-7D85D259E93228407F3D31A9
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-78603A5A87827AE28C28A403
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-586B758F1EABC8361936DC8A
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-78C94573376178A97719C249
      Ten point assessment
      Exact formulation
      Separate renal reference: Open Renal Dosing Master (opens in a new tab)id: multivitamin-injection | generic_name: Multivitamin injection | coverage_status: package_insert_live_plus_legacy_reference | package_insert: query_name: Multivitamin injection | product_and_route_must_match: true | live_current_label_enabled: true | source_priority: 1 | renal: classification: current_label_review_required | summary: Renal dosing status has not been locally normalized; use the current package insert before ordering or administration. | method_note: Use the renal function estimate and body-size convention specified by the selected label or institutional protocol.
      Source IDH51-202851E2C7F5176F81257E30
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-D6F73BD7A95D668CF740C73E
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-20E2DCBA292E39188EA6D1FC
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8337CF25CFAA720ABCD59B07
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-F8DCDE83B655D5DDFA2319C6
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-0B46D09AB5EC7C80B342E87D
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-AF059FF6D872F38A7B5391AA
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-5CFE1A6A25A718BDCD21E7B0
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-5760919785E1A322544EF9FB
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-E972867878F717F0C6FB644D
      Field provenance
      Exact formulation
      Primary
      existing_record_text
      Source IDH51-DFA13AAAADEDF8C20CA8F594
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-0C66AD1FC0202E66574183BF
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-074251441C6A5F6BA859BCA0
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-878E6A8A669DAF44CDE090D0
      Adult dosing range
      Primary
      not_found
      Source IDH51-BA586A4422E827A30C955DDD
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-12254D8A0415528A0A1B065E
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-BC3F13C85E55813B11AF4F55
      Infusion time
      Primary
      not_found
      Source IDH51-7E720D33A270819D254844F2
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-F627DC4AAACBB0ABAB326419
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-B747D1DF06173AE6BD02185A
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-BF361495FF95ACA3573FB360
      Guide generation allowed
      false
      Source IDH51-BA869A529DA47F61FD881708
      Pediatric
      Applicability
      not_established
      Source IDH51-1A85CC2860B9ED51A97ECFD5
      Guide generation allowed
      false
      Source IDH51-FE0DB1096F2CA59D7D833E8E
      Neonatal
      Applicability
      not_established
      Source IDH51-742EA798315235D3C6D456AA
      Guide generation allowed
      false
      Source IDH51-01AF1813E69A4751B4073172
      Route presence
      Structured dilution
      false
      Source IDH51-FDAF9505EF75BC343182D208
      Iv push
      false
      Source IDH51-E6DF25C26EDC106F367BDA5A
      Continuous infusion
      false
      Source IDH51-57ED98DCDDAE723B6C1DD957
      Pediatric source
      false
      Source IDH51-EDCFDC0237AEF4D513CFA47A
      Neonatal source
      false
      Source IDH51-D97F261E68A324DEC9129AF1
      Legacy reference
      Status
      not_available
      Source IDH51-B692D33CB140298B6AB407AF
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-142C1DAB08042B5313D8D921
      Source files
      1. catalog.json
        Source IDH51-3409B44FE853C29F4B1404B5
      2. dosing.json
        Source IDH51-F051A6D378941EE50FCF0EBD
      3. legacy-map.json
        Source IDH51-D69F5B793F301CBAD759F09B
      4. review-queue.json
        Source IDH51-4356F8F3E5C57C9D415EDF01
      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-D04544750CF729BB023E41A5
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-AAA1635A4D74D1759C6A2A17catalog.json
      /records/172/id
      Historical; current review incomplete
      H51-0F18F7CFD2D9C2F8C3BE6406catalog.json
      /records/172/legacy_title
      Historical; current review incomplete
      H51-0BB5F09BD7A8FCFF313C2002catalog.json
      /records/172/generic_name
      Historical; current review incomplete
      H51-0BFE5DCC04C64C0F5F9686CDcatalog.json
      /records/172/class
      Historical; current review incomplete
      H51-07A3E03DD4F14DAB0394AAFEcatalog.json
      /records/172/subclass
      Historical; current review incomplete
      H51-4CFCB80661D6AAF7870C291Dcatalog.json
      /records/172/summary
      Historical; current review incomplete
      H51-9F413ECBDC3292A961EB4579catalog.json
      /records/172/warnings/0
      Historical; current review incomplete
      H51-40F6C8934E61D257828A97BDcatalog.json
      /records/172/stability_notes/0
      Historical; current review incomplete
      H51-3C6106FD52B083887C42FD3Dcatalog.json
      /records/172/populations/0
      Historical; current review incomplete
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