Jantoven - 0832-1215-00 - (Warfarin Sodium)

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Drug Information of Jantoven

Product NDC: 0832-1215
Proprietary Name: Jantoven
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 4    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: 0832-1215
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: 0832-1215-00
Package Description: 100 TABLET in 1 BOTTLE (0832-1215-00)

NDC Information of Jantoven

NDC Code 0832-1215-00
Proprietary Name Jantoven
Package Description 100 TABLET in 1 BOTTLE (0832-1215-00)
Product NDC 0832-1215
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 4
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Jantoven


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