Jantoven - 0832-1216-10 - (Warfarin Sodium)

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Drug Information of Jantoven

Product NDC: 0832-1216
Proprietary Name: Jantoven
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 5    mg/1 & nbsp;   Warfarin Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Jantoven

Product NDC: 0832-1216
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040416
Marketing Category: ANDA
Start Marketing Date: 20100223

Package Information of Jantoven

Package NDC: 0832-1216-10
Package Description: 1000 TABLET in 1 BOTTLE (0832-1216-10)

NDC Information of Jantoven

NDC Code 0832-1216-10
Proprietary Name Jantoven
Package Description 1000 TABLET in 1 BOTTLE (0832-1216-10)
Product NDC 0832-1216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100223
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name WARFARIN SODIUM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Jantoven


General Information