Topiramate - 31722-278-05 - (Topiramate)

Alphabetical Index


Drug Information of Topiramate

Product NDC: 31722-278
Proprietary Name: Topiramate
Non Proprietary Name: Topiramate
Active Ingredient(s): 25    mg/1 & nbsp;   Topiramate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Topiramate

Product NDC: 31722-278
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079162
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Topiramate

Package NDC: 31722-278-05
Package Description: 500 TABLET in 1 BOTTLE (31722-278-05)

NDC Information of Topiramate

NDC Code 31722-278-05
Proprietary Name Topiramate
Package Description 500 TABLET in 1 BOTTLE (31722-278-05)
Product NDC 31722-278
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 Camber Pharmaceuticals
Substance Name TOPIRAMATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Topiramate


General Information