TOPIRAMATE - 54868-6017-0 - (TOPIRAMATE)

Alphabetical Index


Drug Information of TOPIRAMATE

Product NDC: 54868-6017
Proprietary Name: TOPIRAMATE
Non Proprietary Name: TOPIRAMATE
Active Ingredient(s): 50    mg/1 & nbsp;   TOPIRAMATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TOPIRAMATE

Product NDC: 54868-6017
Labeler Name: Physicians Total Care, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090278
Marketing Category: ANDA
Start Marketing Date: 20090506

Package Information of TOPIRAMATE

Package NDC: 54868-6017-0
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (54868-6017-0)

NDC Information of TOPIRAMATE

NDC Code 54868-6017-0
Proprietary Name TOPIRAMATE
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (54868-6017-0)
Product NDC 54868-6017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TOPIRAMATE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090506
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc
Substance Name TOPIRAMATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of TOPIRAMATE


General Information