COUMADIN - 0056-0170-75 - (warfarin sodium)

Alphabetical Index


Drug Information of COUMADIN

Product NDC: 0056-0170
Proprietary Name: COUMADIN
Non Proprietary Name: warfarin sodium
Active Ingredient(s): 2    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: 0056-0170
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: 0056-0170-75
Package Description: 10 BLISTER PACK in 1 CARTON (0056-0170-75) > 10 TABLET in 1 BLISTER PACK (0056-0170-01)

NDC Information of COUMADIN

NDC Code 0056-0170-75
Proprietary Name COUMADIN
Package Description 10 BLISTER PACK in 1 CARTON (0056-0170-75) > 10 TABLET in 1 BLISTER PACK (0056-0170-01)
Product NDC 0056-0170
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 2
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of COUMADIN


General Information