COUMADIN - 55154-7716-0 - (warfarin sodium)

Alphabetical Index


Drug Information of COUMADIN

Product NDC: 55154-7716
Proprietary Name: COUMADIN
Non Proprietary Name: warfarin sodium
Active Ingredient(s): 3    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: 55154-7716
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009218
Marketing Category: NDA
Start Marketing Date: 20090101

Package Information of COUMADIN

Package NDC: 55154-7716-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-7716-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of COUMADIN

NDC Code 55154-7716-0
Proprietary Name COUMADIN
Package Description 10 BLISTER PACK in 1 BAG (55154-7716-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-7716
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 Cardinal Health
Substance Name WARFARIN SODIUM
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of COUMADIN


General Information