warfarin sodium

Generic: warfarin sodium

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name warfarin sodium
Generic Name warfarin sodium
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

warfarin sodium 5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-1721
Product ID 0093-1721_b8c33971-54b3-4971-bf7f-1bec66999a29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040616
Listing Expiration 2026-12-31
Marketing Start 2015-04-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00931721
Hyphenated Format 0093-1721

Supplemental Identifiers

RxCUI
855288 855296 855302 855312 855318 855324 855332 855338 855344
UPC
0300931721013 0300931713018 0300931714015 0300931723017 0300931716019 0300931715012
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 ANDA040616 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-1721-01)
  • 1000 TABLET in 1 BOTTLE (0093-1721-10)
source: ndc

Packages (2)

0093-1721-01 100 TABLET in 1 BOTTLE (0093-1721-01) 0093-1721-10 1000 TABLET in 1 BOTTLE (0093-1721-10)

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": "b8c33971-54b3-4971-bf7f-1bec66999a29", "openfda": {"upc": ["0300931721013", "0300931713018", "0300931714015", "0300931723017", "0300931716019", "0300931715012"], "unii": ["6153CWM0CL"], "rxcui": ["855288", "855296", "855302", "855312", "855318", "855324", "855332", "855338", "855344"], "spl_set_id": ["0cbce382-9c88-4f58-ae0f-532a841e8f95"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-1721-01)", "package_ndc": "0093-1721-01", "marketing_start_date": "20150415"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0093-1721-10)", "package_ndc": "0093-1721-10", "marketing_start_date": "20150407"}], "brand_name": "Warfarin Sodium", "product_id": "0093-1721_b8c33971-54b3-4971-bf7f-1bec66999a29", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "0093-1721", "generic_name": "Warfarin Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Warfarin Sodium", "active_ingredients": [{"name": "WARFARIN SODIUM", "strength": "5 mg/1"}], "application_number": "ANDA040616", "marketing_category": "ANDA", "marketing_start_date": "20150407", "listing_expiration_date": "20261231"}