Levetiracetam

Product NDC

49884-205

11-digit product format

498840205

Labeler code

49884

Product ID

49884-205_8b278c49-8e40-4873-b73d-d5a4a3d6ee3a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levetiracetam

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Par Pharmaceutical Inc.

Application

ANDA091291

Marketing category

ANDA

Marketing start

2011-09-13

Marketing end

0000-00-00

Substance

LEVETIRACETAM

Active strength

750 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record