warfarin sodium
Generic: warfarin sodium
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
warfarin sodium
Generic Name
warfarin sodium
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
warfarin sodium 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-176
Product ID
43063-176_39fd1172-a49a-5ea2-e063-6394a90a7e16
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040616
Listing Expiration
2026-12-31
Marketing Start
2015-04-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063176
Hyphenated Format
43063-176
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 14 TABLET in 1 BOTTLE, PLASTIC (43063-176-14)
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-176-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39fd1172-a49a-5ea2-e063-6394a90a7e16", "openfda": {"upc": ["0343063176306"], "unii": ["6153CWM0CL"], "rxcui": ["855332"], "spl_set_id": ["21255cd5-3c2e-4574-9620-9347d14256b3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-176-14)", "package_ndc": "43063-176-14", "marketing_start_date": "20160203"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-176-30)", "package_ndc": "43063-176-30", "marketing_start_date": "20170905"}], "brand_name": "Warfarin Sodium", "product_id": "43063-176_39fd1172-a49a-5ea2-e063-6394a90a7e16", "dosage_form": "TABLET", "pharm_class": ["Vitamin K Antagonist [EPC]", "Vitamin K Inhibitors [MoA]"], "product_ndc": "43063-176", "generic_name": "Warfarin Sodium", "labeler_name": "PD-Rx Pharmaceuticals, 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"}