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Warfarin Sodium - 63629-4748-3 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 63629-4748
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 4    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: 63629-4748
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040145
Marketing Category: ANDA
Start Marketing Date: 19970725

Package Information of Warfarin Sodium

Package NDC: 63629-4748-3
Package Description: 90 TABLET in 1 BOTTLE (63629-4748-3)

NDC Information of Warfarin Sodium

NDC Code 63629-4748-3
Proprietary Name Warfarin Sodium
Package Description 90 TABLET in 1 BOTTLE (63629-4748-3)
Product NDC 63629-4748
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970725
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name WARFARIN SODIUM
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


General Information