Felbatol - 0037-0431-01 - (felbamate)

Alphabetical Index


Drug Information of Felbatol

Product NDC: 0037-0431
Proprietary Name: Felbatol
Non Proprietary Name: felbamate
Active Ingredient(s): 600    mg/1 & nbsp;   felbamate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Felbatol

Product NDC: 0037-0431
Labeler Name: Meda Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020189
Marketing Category: NDA
Start Marketing Date: 19930729

Package Information of Felbatol

Package NDC: 0037-0431-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01)

NDC Information of Felbatol

NDC Code 0037-0431-01
Proprietary Name Felbatol
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01)
Product NDC 0037-0431
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name felbamate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930729
Marketing Category Name NDA
Labeler Name Meda Pharmaceuticals Inc.
Substance Name FELBAMATE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Felbatol


General Information