Home > National Drug Code (NDC) > Warfarin Sodium

Warfarin Sodium - 51672-4035-3 - (Warfarin Sodium)

Alphabetical Index


Drug Information of Warfarin Sodium

Product NDC: 51672-4035
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 10    mg/1 & nbsp;   Warfarin Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Warfarin Sodium

Product NDC: 51672-4035
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040301
Marketing Category: ANDA
Start Marketing Date: 19990715

Package Information of Warfarin Sodium

Package NDC: 51672-4035-3
Package Description: 1000 TABLET in 1 BOTTLE (51672-4035-3)

NDC Information of Warfarin Sodium

NDC Code 51672-4035-3
Proprietary Name Warfarin Sodium
Package Description 1000 TABLET in 1 BOTTLE (51672-4035-3)
Product NDC 51672-4035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990715
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name WARFARIN SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


General Information