Zonisamide - 0378-6726-01 - (zonisamide)

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Drug Information of Zonisamide

Product NDC: 0378-6726
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: 0378-6726
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077637
Marketing Category: ANDA
Start Marketing Date: 20121022

Package Information of Zonisamide

Package NDC: 0378-6726-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-6726-01)

NDC Information of Zonisamide

NDC Code 0378-6726-01
Proprietary Name Zonisamide
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-6726-01)
Product NDC 0378-6726
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zonisamide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121022
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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