Levetiracetam

Product NDC

68788-6966

11-digit product format

687886966

Labeler code

68788

Product ID

68788-6966_bdd92504-df75-476a-a7fe-f4f49faecf42

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA090843

Marketing category

ANDA

Marketing start

2017-05-18

Marketing end

0000-00-00

Substance

LEVETIRACETAM

Active strength

500 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record