LEVETIRACETAM

Product NDC

40051-135

11-digit product format

400510135

Labeler code

40051

Product ID

40051-135_bfeea4b2-5d36-4ac4-9801-1b3edc9b9975

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levetiracetam

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lotus Pharmaceutical Co., Ltd. Nantou Plant

Application

ANDA090906

Marketing category

ANDA

Marketing start

2017-03-30

Marketing end

0000-00-00

Substance

LEVETIRACETAM

Active strength

250 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record