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Warfarin Sodium - 52125-385-02 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 52125-385
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 10    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: 52125-385
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040301
Marketing Category: ANDA
Start Marketing Date: 20130513

Package Information of Warfarin Sodium

Package NDC: 52125-385-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-385-02)

NDC Information of Warfarin Sodium

NDC Code 52125-385-02
Proprietary Name Warfarin Sodium
Package Description 30 TABLET in 1 BLISTER PACK (52125-385-02)
Product NDC 52125-385
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130513
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name WARFARIN SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


General Information