COUMADIN - 52125-080-02 - (warfarin sodium)

Alphabetical Index


Drug Information of COUMADIN

Product NDC: 52125-080
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: 52125-080
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009218
Marketing Category: NDA
Start Marketing Date: 20130226

Package Information of COUMADIN

Package NDC: 52125-080-02
Package Description: 100 TABLET in 1 BLISTER PACK (52125-080-02)

NDC Information of COUMADIN

NDC Code 52125-080-02
Proprietary Name COUMADIN
Package Description 100 TABLET in 1 BLISTER PACK (52125-080-02)
Product NDC 52125-080
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name warfarin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130226
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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