Zonisamide

Product NDC

0185-0199

11-digit product format

001850199

Labeler code

0185

Product ID

0185-0199_7e7898d4-7d5a-44cd-9087-9445695ded53

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Zonisamide

Dosage form

CAPSULE

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA077644

Marketing category

ANDA

Marketing start

2005-12-22

Marketing end

0000-00-00

Substance

ZONISAMIDE

Active strength

50 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

2019-12-31

Current FDA listing

Historical FDA.report record