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United States · US · US:71335-2309_fbf1e034-ee7f-4f4a-84d3-a5ea78fdd363

Warfarin Sodium

Orange BookUNIISPLATC B01AA03

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

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
    7133523091
    30 TABLET in 1 BOTTLE (71335-2309-1)
  • ndc11
    7133523092
    14 TABLET in 1 BOTTLE (71335-2309-2)
  • ndc11
    7133523093
    90 TABLET in 1 BOTTLE (71335-2309-3)
  • ndc11
    7133523094
    45 TABLET in 1 BOTTLE (71335-2309-4)
  • ndc11
    7133523095
    50 TABLET in 1 BOTTLE (71335-2309-5)
  • ndc11
    7133523096
    21 TABLET in 1 BOTTLE (71335-2309-6)
  • ndc11
    7133523097
    60 TABLET in 1 BOTTLE (71335-2309-7)
  • ndc11
    7133523098
    20 TABLET in 1 BOTTLE (71335-2309-8)

Annotations

UNII (FDA Substance ID)
6153CWM0CL
WARFARIN SODIUM
RxCUI 114194
Orange Book
A202202
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": "71335-2309_fbf1e034-ee7f-4f4a-84d3-a5ea78fdd363",
  "productndc": "71335-2309",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202202",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "001",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "002",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "003",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "3MG",
        "product_no": "004",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "4MG",
        "product_no": "005",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "006",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "007",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "008",
        "approval_date": "Mar 4, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "009",
        "approval_date": "Mar 4, 2013"
      }
    ],
    "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": "ANDA202202",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Warfarin",
  "start_marketing_date": "20100816",
  "active_numerator_strength": "2"
}

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