Zonisamide - 0185-0199-01 - (Zonisamide)

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Drug Information of Zonisamide

Product NDC: 0185-0199
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: 0185-0199
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077644
Marketing Category: ANDA
Start Marketing Date: 20051222

Package Information of Zonisamide

Package NDC: 0185-0199-01
Package Description: 100 CAPSULE in 1 BOTTLE (0185-0199-01)

NDC Information of Zonisamide

NDC Code 0185-0199-01
Proprietary Name Zonisamide
Package Description 100 CAPSULE in 1 BOTTLE (0185-0199-01)
Product NDC 0185-0199
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zonisamide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20051222
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
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