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 10 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-210
Product ID 72189-210_2be9877c-0b1d-23b4-e063-6394a90af68f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090935
Listing Expiration 2026-12-31
Marketing Start 2021-05-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189210
Hyphenated Format 72189-210

Supplemental Identifiers

RxCUI
855296
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
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72189-210-71)
source: ndc

Packages (1)

72189-210-71 100 TABLET in 1 BOTTLE (72189-210-71)

Ingredients (1)

warfarin sodium (10 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": "2be9877c-0b1d-23b4-e063-6394a90af68f", "openfda": {"unii": ["6153CWM0CL"], "rxcui": ["855296"], "spl_set_id": ["c186d1ff-64dd-bfcb-e053-2a95a90af800"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72189-210-71)", "package_ndc": "72189-210-71", "marketing_start_date": "20210504"}], "brand_name": "WARFARIN SODIUM", "product_id": "72189-210_2be9877c-0b1d-23b4-e063-6394a90af68f", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "72189-210", "generic_name": "WARFARIN SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "WARFARIN SODIUM", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA090935", "marketing_category": "ANDA", "marketing_start_date": "20210504", "listing_expiration_date": "20261231"}