Levetiracetam

Product NDC

51079-822

11-digit product format

510790822

Labeler code

51079

Product ID

51079-822_9aee1f84-b441-09a6-e053-2a95a90ae4d8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076919

Marketing category

ANDA

Marketing start

2008-11-04

Marketing end

2020-05-31

Substance

LEVETIRACETAM

Active strength

750 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record