warfarin sodium

Generic: warfarin sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name warfarin sodium
Generic Name warfarin sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

warfarin sodium 5 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-4032
Product ID 51672-4032_373f3fe2-c159-028e-e063-6394a90aff59
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040301
Listing Expiration 2026-12-31
Marketing Start 1999-07-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724032
Hyphenated Format 51672-4032

Supplemental Identifiers

RxCUI
855288 855296 855302 855312 855318 855324 855332 855338 855344
UPC
0351672402815 0351672403416 0351672402914 0351672403119 0351672403218 0351672403010 0351672403515 0351672403317
UNII
6153CWM0CL

Packaging Origin

Original Packager
true

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 ANDA040301 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (51672-4032-1)
  • 1000 TABLET in 1 BOTTLE (51672-4032-3)
  • 5000 TABLET in 1 BOTTLE (51672-4032-7)
source: ndc

Packages (3)

51672-4032-1 100 TABLET in 1 BOTTLE (51672-4032-1) 51672-4032-3 1000 TABLET in 1 BOTTLE (51672-4032-3) 51672-4032-7 5000 TABLET in 1 BOTTLE (51672-4032-7)

Ingredients (1)

warfarin sodium (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": "373f3fe2-c159-028e-e063-6394a90aff59", "openfda": {"upc": ["0351672402815", "0351672403416", "0351672402914", "0351672403119", "0351672403218", "0351672403010", "0351672403515", "0351672403317"], "unii": ["6153CWM0CL"], "rxcui": ["855288", "855296", "855302", "855312", "855318", "855324", "855332", "855338", "855344"], "spl_set_id": ["8ad881e0-ca41-42ad-9d7d-eb85b3a30af0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4032-1)", "package_ndc": "51672-4032-1", "marketing_start_date": "19990715"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4032-3)", "package_ndc": "51672-4032-3", "marketing_start_date": "19990715"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (51672-4032-7)", "package_ndc": "51672-4032-7", "marketing_start_date": "19990715"}], "brand_name": "Warfarin Sodium", "product_id": "51672-4032_373f3fe2-c159-028e-e063-6394a90aff59", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "51672-4032", "generic_name": "Warfarin Sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "5 mg/1"}], "application_number": "ANDA040301", "marketing_category": "ANDA", "marketing_start_date": "19990715", "listing_expiration_date": "20261231"}