TOPIRAMATE - 52125-047-02 - (topiramate)

Alphabetical Index


Drug Information of TOPIRAMATE

Product NDC: 52125-047
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: 52125-047
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079153
Marketing Category: ANDA
Start Marketing Date: 20130401

Package Information of TOPIRAMATE

Package NDC: 52125-047-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-047-02)

NDC Information of TOPIRAMATE

NDC Code 52125-047-02
Proprietary Name TOPIRAMATE
Package Description 30 TABLET in 1 BLISTER PACK (52125-047-02)
Product NDC 52125-047
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name topiramate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130401
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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