Topiramate - 16252-568-60 - (Topiramate)

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Drug Information of Topiramate

Product NDC: 16252-568
Proprietary Name: Topiramate
Non Proprietary Name: Topiramate
Active Ingredient(s): 15    mg/1 & nbsp;   Topiramate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, COATED PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Topiramate

Product NDC: 16252-568
Labeler Name: Cobalt Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077868
Marketing Category: ANDA
Start Marketing Date: 20090415

Package Information of Topiramate

Package NDC: 16252-568-60
Package Description: 60 CAPSULE, COATED PELLETS in 1 BOTTLE, PLASTIC (16252-568-60)

NDC Information of Topiramate

NDC Code 16252-568-60
Proprietary Name Topiramate
Package Description 60 CAPSULE, COATED PELLETS in 1 BOTTLE, PLASTIC (16252-568-60)
Product NDC 16252-568
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Topiramate
Dosage Form Name CAPSULE, COATED PELLETS
Route Name ORAL
Start Marketing Date 20090415
Marketing Category Name ANDA
Labeler Name Cobalt Laboratories
Substance Name TOPIRAMATE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Topiramate


General Information