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Warfarin Sodium - 51138-061-30 - (warfarin sodium)

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Drug Information of Warfarin Sodium

Product NDC: 51138-061
Proprietary Name: Warfarin Sodium
Non Proprietary Name: warfarin sodium
Active Ingredient(s): 7.5    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: 51138-061
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040301
Marketing Category: ANDA
Start Marketing Date: 20110209

Package Information of Warfarin Sodium

Package NDC: 51138-061-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (51138-061-30)

NDC Information of Warfarin Sodium

NDC Code 51138-061-30
Proprietary Name Warfarin Sodium
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (51138-061-30)
Product NDC 51138-061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name warfarin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110209
Marketing Category Name ANDA
Labeler Name Med-Health Pharma, LLC
Substance Name WARFARIN SODIUM
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


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