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Warfarin Sodium - 35356-582-60 - (Warfarin Sodium)

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Drug Information of Warfarin Sodium

Product NDC: 35356-582
Proprietary Name: Warfarin Sodium
Non Proprietary Name: Warfarin Sodium
Active Ingredient(s): 1    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: 35356-582
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040663
Marketing Category: ANDA
Start Marketing Date: 20060530

Package Information of Warfarin Sodium

Package NDC: 35356-582-60
Package Description: 60 TABLET in 1 BOTTLE (35356-582-60)

NDC Information of Warfarin Sodium

NDC Code 35356-582-60
Proprietary Name Warfarin Sodium
Package Description 60 TABLET in 1 BOTTLE (35356-582-60)
Product NDC 35356-582
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Warfarin Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060530
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name WARFARIN SODIUM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]

Complete Information of Warfarin Sodium


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