Felbamate - 51525-0442-3 - (felbamate)

Alphabetical Index


Drug Information of Felbamate

Product NDC: 51525-0442
Proprietary Name: Felbamate
Non Proprietary Name: felbamate
Active Ingredient(s): 600    mg/5mL & nbsp;   felbamate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Felbamate

Product NDC: 51525-0442
Labeler Name: Wallace Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020189
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111123

Package Information of Felbamate

Package NDC: 51525-0442-3
Package Description: 946 mL in 1 BOTTLE (51525-0442-3)

NDC Information of Felbamate

NDC Code 51525-0442-3
Proprietary Name Felbamate
Package Description 946 mL in 1 BOTTLE (51525-0442-3)
Product NDC 51525-0442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name felbamate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20111123
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Wallace Pharmaceuticals Inc.
Substance Name FELBAMATE
Strength Number 600
Strength Unit mg/5mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Felbamate


General Information