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Warfarin Sodium - 67544-318-70 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 67544-318
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 2    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: 67544-318
Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040301
Marketing Category: ANDA
Start Marketing Date: 19990715

Package Information of Warfarin Sodium

Package NDC: 67544-318-70
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (67544-318-70)

NDC Information of Warfarin Sodium

NDC Code 67544-318-70
Proprietary Name Warfarin Sodium
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (67544-318-70)
Product NDC 67544-318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990715
Marketing Category Name ANDA
Labeler Name Aphena Pharma Solutions - Tennessee, Inc.
Substance Name WARFARIN SODIUM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


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