COUMADIN - 0056-0172-70 - (warfarin sodium)

Alphabetical Index


Drug Information of COUMADIN

Product NDC: 0056-0172
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: 0056-0172
Labeler Name: Bristol-Myers Squibb Pharma Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009218
Marketing Category: NDA
Start Marketing Date: 20090101

Package Information of COUMADIN

Package NDC: 0056-0172-70
Package Description: 1 BOTTLE in 1 CARTON (0056-0172-70) > 100 TABLET in 1 BOTTLE

NDC Information of COUMADIN

NDC Code 0056-0172-70
Proprietary Name COUMADIN
Package Description 1 BOTTLE in 1 CARTON (0056-0172-70) > 100 TABLET in 1 BOTTLE
Product NDC 0056-0172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name warfarin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090101
Marketing Category Name NDA
Labeler Name Bristol-Myers Squibb Pharma Company
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