Topamax - 21695-130-15 - (topiramate)

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Drug Information of Topamax

Product NDC: 21695-130
Proprietary Name: Topamax
Non Proprietary Name: topiramate
Active Ingredient(s): 100    mg/1 & nbsp;   topiramate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Topamax

Product NDC: 21695-130
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020505
Marketing Category: NDA
Start Marketing Date: 19970101

Package Information of Topamax

Package NDC: 21695-130-15
Package Description: 15 TABLET, COATED in 1 BOTTLE (21695-130-15)

NDC Information of Topamax

NDC Code 21695-130-15
Proprietary Name Topamax
Package Description 15 TABLET, COATED in 1 BOTTLE (21695-130-15)
Product NDC 21695-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name topiramate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19970101
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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 Topamax


General Information