Lamotrigine

Product NDC

0093-0132

11-digit product format

000930132

Labeler code

0093

Product ID

0093-0132_ab3cf2de-a729-47a2-a842-ab5bdaf72dca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lamotrigine

Dosage form

TABLET, CHEWABLE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA076420

Marketing category

ANDA

Marketing start

2006-06-29

Marketing end

2019-07-31

Substance

LAMOTRIGINE

Active strength

25 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Anti-epileptic Agent [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record