Topiramate - 0093-0155-06 - (Topiramate)

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Drug Information of Topiramate

Product NDC: 0093-0155
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: 0093-0155
Labeler Name: TEVA Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076317
Marketing Category: ANDA
Start Marketing Date: 20090331

Package Information of Topiramate

Package NDC: 0093-0155-06
Package Description: 60 TABLET in 1 BOTTLE (0093-0155-06)

NDC Information of Topiramate

NDC Code 0093-0155-06
Proprietary Name Topiramate
Package Description 60 TABLET in 1 BOTTLE (0093-0155-06)
Product NDC 0093-0155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Topiramate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090331
Marketing Category Name ANDA
Labeler Name TEVA Pharmaceuticals USA 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