LAMOTRIGINE

Product NDC

50090-3278

11-digit product format

500903278

Labeler code

50090

Product ID

50090-3278_6f490b75-0bf7-4be2-989d-e5fee1a1d8b5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lamotrigine

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077783

Marketing category

ANDA

Marketing start

2010-11-01

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

2019-12-31

Current FDA listing

Historical FDA.report record