TOPIRAMATE - 13668-034-77 - (topiramate)

Alphabetical Index


Drug Information of TOPIRAMATE

Product NDC: 13668-034
Proprietary Name: TOPIRAMATE
Non Proprietary Name: topiramate
Active Ingredient(s): 200    mg/1 & nbsp;   topiramate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of TOPIRAMATE

Product NDC: 13668-034
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079153
Marketing Category: ANDA
Start Marketing Date: 20090327

Package Information of TOPIRAMATE

Package NDC: 13668-034-77
Package Description: 80 TABLET in 1 DOSE PACK (13668-034-77)

NDC Information of TOPIRAMATE

NDC Code 13668-034-77
Proprietary Name TOPIRAMATE
Package Description 80 TABLET in 1 DOSE PACK (13668-034-77)
Product NDC 13668-034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name topiramate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090327
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name TOPIRAMATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of TOPIRAMATE


General Information