warfarin sodium

Generic: warfarin sodium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name warfarin sodium
Generic Name warfarin sodium
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

warfarin sodium 3 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2230
Product ID 72162-2230_4a06b3c4-8a13-4eb1-862d-856885e27641
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090935
Listing Expiration 2026-12-31
Marketing Start 2011-11-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622230
Hyphenated Format 72162-2230

Supplemental Identifiers

RxCUI
855318
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 ANDA090935 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72162-2230-0)
source: ndc

Packages (1)

72162-2230-0 1000 TABLET in 1 BOTTLE (72162-2230-0)

Ingredients (1)

warfarin sodium (3 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": "4a06b3c4-8a13-4eb1-862d-856885e27641", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855318"], "spl_set_id": ["f827bb9a-6afd-4d0c-a7ca-bdef0667be52"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2230-0)", "package_ndc": "72162-2230-0", "marketing_start_date": "20240126"}], "brand_name": "Warfarin Sodium", "product_id": "72162-2230_4a06b3c4-8a13-4eb1-862d-856885e27641", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "72162-2230", "generic_name": "warfarin sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "3 mg/1"}], "application_number": "ANDA090935", "marketing_category": "ANDA", "marketing_start_date": "20111111", "listing_expiration_date": "20261231"}