Jantoven - 55154-5618-0 - (Warfarin Sodium)

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Drug Information of Jantoven

Product NDC: 55154-5618
Proprietary Name: Jantoven
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 Jantoven

Product NDC: 55154-5618
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040416
Marketing Category: ANDA
Start Marketing Date: 20100223

Package Information of Jantoven

Package NDC: 55154-5618-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5618-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Jantoven

NDC Code 55154-5618-0
Proprietary Name Jantoven
Package Description 10 BLISTER PACK in 1 BAG (55154-5618-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5618
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 Cardinal Health
Substance Name WARFARIN SODIUM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Jantoven


General Information