LEVETIRACETAM Extended-release

Product NDC

40051-332

11-digit product format

400510332

Labeler code

40051

Product ID

40051-332_7c902b2c-edf6-4dd0-923f-c38f2c621733

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

levetiracetam

Dosage form

TABLET

Route

ORAL

Labeler

Lotus Pharmaceutical Co., Ltd. Nantou Plant

Application

ANDA202095

Marketing category

ANDA

Marketing start

2016-10-31

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

2017-12-31

Current FDA listing

Historical FDA.report record