Levetiracetam

Product NDC

0591-3635

11-digit product format

005913635

Labeler code

0591

Product ID

0591-3635_392da1d3-de2e-46f0-b88b-1859c40dbb62

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levetiracetam

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA091093

Marketing category

ANDA

Marketing start

2011-09-12

Marketing end

2019-03-31

Substance

LEVETIRACETAM

Active strength

500 mg/1

Pharmacologic classes

Decreased Centr

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record