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Warfarin Sodium - 51672-4027-0 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 51672-4027
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 1    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: 51672-4027
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: 51672-4027-0
Package Description: 10 BLISTER PACK in 1 CARTON (51672-4027-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Warfarin Sodium

NDC Code 51672-4027-0
Proprietary Name Warfarin Sodium
Package Description 10 BLISTER PACK in 1 CARTON (51672-4027-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 51672-4027
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 1
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


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