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Warfarin Sodium - 55154-0879-9 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 55154-0879
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 4    mg/1 & nbsp;   Warfarin Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Warfarin Sodium

Product NDC: 55154-0879
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040145
Marketing Category: ANDA
Start Marketing Date: 20100329

Package Information of Warfarin Sodium

Package NDC: 55154-0879-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-0879-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Warfarin Sodium

NDC Code 55154-0879-9
Proprietary Name Warfarin Sodium
Package Description 6 BLISTER PACK in 1 CARTON (55154-0879-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-0879
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100329
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name WARFARIN SODIUM
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


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