Levetiracetam

Product NDC

70518-1482

11-digit product format

705181482

Labeler code

70518

Product ID

70518-1482_93c19825-4ff6-178b-e053-2a95a90a5dc9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078154

Marketing category

ANDA

Marketing start

2018-10-06

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

2020-12-31

Current FDA listing

Historical FDA.report record