Zonisamide - 68462-128-05 - (Zonisamide)

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Drug Information of Zonisamide

Product NDC: 68462-128
Proprietary Name: Zonisamide
Non Proprietary Name: Zonisamide
Active Ingredient(s): 25    mg/1 & nbsp;   Zonisamide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zonisamide

Product NDC: 68462-128
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077651
Marketing Category: ANDA
Start Marketing Date: 20060130

Package Information of Zonisamide

Package NDC: 68462-128-05
Package Description: 500 CAPSULE in 1 BOTTLE (68462-128-05)

NDC Information of Zonisamide

NDC Code 68462-128-05
Proprietary Name Zonisamide
Package Description 500 CAPSULE in 1 BOTTLE (68462-128-05)
Product NDC 68462-128
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zonisamide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060130
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name ZONISAMIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Zonisamide


General Information