warfarin sodium

Generic: warfarin sodium

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name warfarin sodium
Generic Name warfarin sodium
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

warfarin sodium 4 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-405
Product ID 72189-405_2c4ced46-ac01-014b-e063-6394a90a5a5d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202202
Listing Expiration 2026-12-31
Marketing Start 2022-12-15

Pharmacologic Class

Classes
vitamin k antagonist [epc] vitamin k inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189405
Hyphenated Format 72189-405

Supplemental Identifiers

RxCUI
855324
UNII
6153CWM0CL

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name warfarin sodium (source: ndc)
Generic Name warfarin sodium (source: ndc)
Application Number ANDA202202 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72189-405-71)
source: ndc

Packages (1)

72189-405-71 100 TABLET in 1 BOTTLE (72189-405-71)

Ingredients (1)

warfarin sodium (4 mg/1)

Linked Drug Pages (1)

WARFARIN SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4ced46-ac01-014b-e063-6394a90a5a5d", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855324"], "spl_set_id": ["efded00a-22b9-1da7-e053-2995a90a58ca"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72189-405-71)", "package_ndc": "72189-405-71", "marketing_start_date": "20221215"}], "brand_name": "WARFARIN SODIUM", "product_id": "72189-405_2c4ced46-ac01-014b-e063-6394a90a5a5d", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "72189-405", "generic_name": "WARFARIN SODIUM", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "WARFARIN SODIUM", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "4 mg/1"}], "application_number": "ANDA202202", "marketing_category": "ANDA", "marketing_start_date": "20221215", "listing_expiration_date": "20261231"}