Levetiracetam

Product NDC

51079-820

11-digit product format

510790820

Labeler code

51079

Product ID

51079-820_7c75ad05-4de4-6185-e053-2a91aa0a25e9

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

0000-00-00

Substance

LEVETIRACETAM

Active strength

250 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record