Zonisamide

Product NDC

51079-768

11-digit product format

510790768

Labeler code

51079

Product ID

51079-768_7d8f6709-56bc-6f59-e053-2a91aa0a5bf4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

zonisamide

Dosage form

CAPSULE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA077637

Marketing category

ANDA

Marketing start

2006-01-25

Marketing end

2019-06-30

Substance

ZONISAMIDE

Active strength

100 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE],Anti-epileptic Agent [EPC],Sulfonamides [CS],Carbonic Anhydrase Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record