ZONISAMIDE - 64679-946-01 - (ZONISAMIDE)

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Drug Information of ZONISAMIDE

Product NDC: 64679-946
Proprietary Name: ZONISAMIDE
Non Proprietary Name: ZONISAMIDE
Active Ingredient(s): 50    mg/1 & nbsp;   ZONISAMIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of ZONISAMIDE

Product NDC: 64679-946
Labeler Name: WOCKHARDT USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077636
Marketing Category: ANDA
Start Marketing Date: 20060727

Package Information of ZONISAMIDE

Package NDC: 64679-946-01
Package Description: 100 CAPSULE in 1 BOTTLE (64679-946-01)

NDC Information of ZONISAMIDE

NDC Code 64679-946-01
Proprietary Name ZONISAMIDE
Package Description 100 CAPSULE in 1 BOTTLE (64679-946-01)
Product NDC 64679-946
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ZONISAMIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060727
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC.
Substance Name ZONISAMIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of ZONISAMIDE


General Information