Topiramate - 49349-802-02 - (Topiramate)

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Drug Information of Topiramate

Product NDC: 49349-802
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: 49349-802
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079162
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of Topiramate

Package NDC: 49349-802-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-802-02)

NDC Information of Topiramate

NDC Code 49349-802-02
Proprietary Name Topiramate
Package Description 30 TABLET in 1 BLISTER PACK (49349-802-02)
Product NDC 49349-802
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Topiramate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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