Levetiracetam

Product NDC

70518-0125

11-digit product format

705180125

Labeler code

70518

Product ID

70518-0125_4a172655-5c28-36f0-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077319

Marketing category

ANDA

Marketing start

2017-01-16

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