Levetiracetam

Product NDC

68788-6838

11-digit product format

687886838

Labeler code

68788

Product ID

68788-6838_2aec2569-e853-47e5-889a-c7ccebf8ecc0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA078154

Marketing category

ANDA

Marketing start

2016-12-05

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record