Levetiracetam

Product NDC

50436-5605

11-digit product format

504365605

Labeler code

50436

Product ID

50436-5605_32204496-6dce-422d-8550-0f225af40a68

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA078154

Marketing category

ANDA

Marketing start

2009-01-01

Marketing end

0000-00-00

Substance

LEVETIRACETAM

Active strength

750 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