COUMADIN - 54868-1259-0 - (warfarin sodium)

Alphabetical Index


Drug Information of COUMADIN

Product NDC: 54868-1259
Proprietary Name: COUMADIN
Non Proprietary Name: warfarin sodium
Active Ingredient(s): 5    mg/1 & nbsp;   warfarin sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of COUMADIN

Product NDC: 54868-1259
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009218
Marketing Category: NDA
Start Marketing Date: 20041115

Package Information of COUMADIN

Package NDC: 54868-1259-0
Package Description: 20 TABLET in 1 BOTTLE (54868-1259-0)

NDC Information of COUMADIN

NDC Code 54868-1259-0
Proprietary Name COUMADIN
Package Description 20 TABLET in 1 BOTTLE (54868-1259-0)
Product NDC 54868-1259
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name warfarin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041115
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name WARFARIN SODIUM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of COUMADIN


General Information