Topiramate - 52125-061-02 - (Topiramate)

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Drug Information of Topiramate

Product NDC: 52125-061
Proprietary Name: Topiramate
Non Proprietary Name: Topiramate
Active Ingredient(s): 25    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: 52125-061
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077627
Marketing Category: ANDA
Start Marketing Date: 20130226

Package Information of Topiramate

Package NDC: 52125-061-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-061-02)

NDC Information of Topiramate

NDC Code 52125-061-02
Proprietary Name Topiramate
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-061-02)
Product NDC 52125-061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Topiramate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130226
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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