Lamotrigine

Product NDC

50436-3995

11-digit product format

504363995

Labeler code

50436

Product ID

50436-3995_0720797a-7f77-4eae-be44-1bcc5e333d24

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lamotrigine

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA079132

Marketing category

ANDA

Marketing start

2009-01-27

Marketing end

0000-00-00

Substance

LAMOTRIGINE

Active strength

100 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

2019-12-31

Current FDA listing

Historical FDA.report record