Warfarin Sodium

Orange BookUNIISPLATC B01AA03

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeB01AA03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133506371
30 TABLET in 1 BOTTLE (71335-0637-1)
ndc11
7133506372
14 TABLET in 1 BOTTLE (71335-0637-2)
ndc11
7133506373
90 TABLET in 1 BOTTLE (71335-0637-3)
ndc11
7133506374
45 TABLET in 1 BOTTLE (71335-0637-4)
ndc11
7133506375
50 TABLET in 1 BOTTLE (71335-0637-5)
ndc11
7133506376
21 TABLET in 1 BOTTLE (71335-0637-6)
ndc11
7133506377
60 TABLET in 1 BOTTLE (71335-0637-7)
ndc11
7133506378
20 TABLET in 1 BOTTLE (71335-0637-8)

Annotations

UNII (FDA Substance ID)

6153CWM0CL

WARFARIN SODIUM

RxCUI 114194

Orange Book

A040616

ABABABABABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6153CWM0CL",
    "rxcui": "114194",
    "inchikey": "KYITYFHKDODNCQ-UHFFFAOYSA-M",
    "display_name": "WARFARIN SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "52bacf1e-9ba8-7eca-e063-6394a90ab60b": {
      "match": "brand_token",
      "title": "WARFARIN SODIUM (WARFARIN) TABLET [COUPLER LLC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71335-0637_491f715c-a6b2-4d04-85e1-893efa4535e2",
  "productndc": "71335-0637",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040616",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "001",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "002",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "3MG",
        "product_no": "003",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "004",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "005",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "006",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "007",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "008",
        "approval_date": "Jul 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "009",
        "approval_date": "Jul 5, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "WARFARIN SODIUM",
  "proprietary_name": "Warfarin Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040616",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Warfarin Sodium",
  "start_marketing_date": "20150505",
  "active_numerator_strength": "2"
}

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