Felbamate - 65162-734-50 - (Felbamate)

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Drug Information of Felbamate

Product NDC: 65162-734
Proprietary Name: Felbamate
Non Proprietary Name: Felbamate
Active Ingredient(s): 400    mg/1 & nbsp;   Felbamate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Felbamate

Product NDC: 65162-734
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201680
Marketing Category: ANDA
Start Marketing Date: 20110916

Package Information of Felbamate

Package NDC: 65162-734-50
Package Description: 500 TABLET in 1 BOTTLE (65162-734-50)

NDC Information of Felbamate

NDC Code 65162-734-50
Proprietary Name Felbamate
Package Description 500 TABLET in 1 BOTTLE (65162-734-50)
Product NDC 65162-734
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Felbamate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110916
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name FELBAMATE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Felbamate


General Information