Lamotrigine

Product NDC

63739-517

11-digit product format

637390517

Labeler code

63739

Product ID

63739-517_79788bb9-6fb6-4193-aaa5-b1441021ccb3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lamotrigine

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA090607

Marketing category

ANDA

Marketing start

2011-06-08

Marketing end

0000-00-00

Substance

LAMOTRIGINE

Active strength

200 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

2020-12-31

Current FDA listing

Historical FDA.report record