Topiramate - 50436-9951-1 - (Topiramate)

Alphabetical Index


Drug Information of Topiramate

Product NDC: 50436-9951
Proprietary Name: Topiramate
Non Proprietary Name: Topiramate
Active Ingredient(s): 100    mg/1 & nbsp;   Topiramate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Topiramate

Product NDC: 50436-9951
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079162
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Topiramate

Package NDC: 50436-9951-1
Package Description: 60 TABLET in 1 BOTTLE (50436-9951-1)

NDC Information of Topiramate

NDC Code 50436-9951-1
Proprietary Name Topiramate
Package Description 60 TABLET in 1 BOTTLE (50436-9951-1)
Product NDC 50436-9951
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Topiramate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name TOPIRAMATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Topiramate


General Information