Zonisamide

Product NDC

43063-575

11-digit product format

430630575

Labeler code

43063

Product ID

43063-575_9595a664-b73f-d726-e053-2995a90a2043

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

zonisamide

Dosage form

CAPSULE

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA077637

Marketing category

ANDA

Marketing start

2005-12-23

Marketing end

0000-00-00

Substance

ZONISAMIDE

Active strength

25 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

2020-12-31

Current FDA listing

Historical FDA.report record