warfarin sodium

Generic: warfarin

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

warfarin sodium 7.5 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1525
Product ID 67046-1525_2f211964-aa77-7efa-e063-6294a90ac902
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202202
Listing Expiration 2026-12-31
Marketing Start 2025-02-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461525
Hyphenated Format 67046-1525

Supplemental Identifiers

RxCUI
855344
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 (source: ndc)
Application Number ANDA202202 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1525-3)
source: ndc

Packages (1)

67046-1525-3 30 TABLET in 1 BLISTER PACK (67046-1525-3)

Ingredients (1)

warfarin sodium (7.5 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": "2f211964-aa77-7efa-e063-6294a90ac902", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855344"], "spl_set_id": ["2f2119e8-f583-ba16-e063-6394a90a13a2"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1525-3)", "package_ndc": "67046-1525-3", "marketing_start_date": "20250227"}], "brand_name": "Warfarin Sodium", "product_id": "67046-1525_2f211964-aa77-7efa-e063-6294a90ac902", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "67046-1525", "generic_name": "Warfarin", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "7.5 mg/1"}], "application_number": "ANDA202202", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}