Zonisamide - 31722-228-01 - (Zonisamide)

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Drug Information of Zonisamide

Product NDC: 31722-228
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: 31722-228
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077869
Marketing Category: ANDA
Start Marketing Date: 20120221

Package Information of Zonisamide

Package NDC: 31722-228-01
Package Description: 24 BOTTLE in 1 CASE (31722-228-01) > 100 CAPSULE in 1 BOTTLE

NDC Information of Zonisamide

NDC Code 31722-228-01
Proprietary Name Zonisamide
Package Description 24 BOTTLE in 1 CASE (31722-228-01) > 100 CAPSULE in 1 BOTTLE
Product NDC 31722-228
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zonisamide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120221
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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