Levetiracetam

Product NDC

50268-475

11-digit product format

502680475

Labeler code

50268

Product ID

50268-475_9c96ef33-7fb5-49fd-e053-2a95a90a24ec

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvPAK

Application

ANDA078106

Marketing category

ANDA

Marketing start

2017-06-13

Marketing end

0000-00-00

Substance

LEVETIRACETAM

Active strength

1000 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record