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United States · US · US:71335-1802_8581b1aa-ce40-4d11-9191-ad7a23ddeb94

Colchicine

Orange BookUNIISPLATC M04AC01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM04AC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 8

  • ndc11
    7133518021
    30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-1)
  • ndc11
    7133518022
    20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-2)
  • ndc11
    7133518023
    3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-3)
  • ndc11
    7133518024
    12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-4)
  • ndc11
    7133518025
    6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-5)
  • ndc11
    7133518026
    9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-6)
  • ndc11
    7133518027
    15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-7)
  • ndc11
    7133518028
    10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1802-8)

Annotations

UNII (FDA Substance ID)
SML2Y3J35T
COLCHICINE
RxCUI 2683
Orange Book
N022352
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "SML2Y3J35T",
    "rxcui": "2683",
    "inchikey": "IAKHMKGGTNLKSZ-INIZCTEOSA-N",
    "display_name": "COLCHICINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "68d4bf2b-8e2c-4621-aa08-463f43e253c3": {
      "match": "brand_token",
      "title": "COLCHICINE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "2",
      "published_date": "2026-05-22"
    }
  },
  "productid": "71335-1802_8581b1aa-ce40-4d11-9191-ad7a23ddeb94",
  "productndc": "71335-1802",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "022352",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "0.6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "001",
        "approval_date": "Jul 29, 2009"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "COLCHICINE",
  "proprietary_name": "Colchicine",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA022352",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "Colchicine",
  "start_marketing_date": "20180701",
  "active_numerator_strength": ".6"
}

Related drugs

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