Lamotrigine

Product NDC

50268-463

11-digit product format

502680463

Labeler code

50268

Product ID

50268-463_6f3c6f7e-066e-0c12-e053-2a91aa0a0759

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lamotrigine

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA079132

Marketing category

ANDA

Marketing start

2015-06-25

Marketing end

0000-00-00

Substance

LAMOTRIGINE

Active strength

150 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