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Warfarin Sodium - 31722-330-10 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 31722-330
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 3    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: 31722-330
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090935
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of Warfarin Sodium

Package NDC: 31722-330-10
Package Description: 1000 TABLET in 1 BOTTLE (31722-330-10)

NDC Information of Warfarin Sodium

NDC Code 31722-330-10
Proprietary Name Warfarin Sodium
Package Description 1000 TABLET in 1 BOTTLE (31722-330-10)
Product NDC 31722-330
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
Substance Name WARFARIN SODIUM
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


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