Zonisamide - 54868-5789-0 - (Zonisamide)

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Drug Information of Zonisamide

Product NDC: 54868-5789
Proprietary Name: Zonisamide
Non Proprietary Name: Zonisamide
Active Ingredient(s): 100    mg/1 & nbsp;   Zonisamide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zonisamide

Product NDC: 54868-5789
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077634
Marketing Category: ANDA
Start Marketing Date: 20070711

Package Information of Zonisamide

Package NDC: 54868-5789-0
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-5789-0)

NDC Information of Zonisamide

NDC Code 54868-5789-0
Proprietary Name Zonisamide
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-5789-0)
Product NDC 54868-5789
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zonisamide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070711
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ZONISAMIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Zonisamide


General Information