ZONISAMIDE

Product NDC

63629-5008

11-digit product format

636295008

Labeler code

63629

Product ID

63629-5008_5ff7324f-e0aa-44fe-8f3f-016983c4f4f0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ZONISAMIDE

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077636

Marketing category

ANDA

Marketing start

2006-07-27

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record