Felbamate

Product NDC

47781-551

11-digit product format

477810551

Labeler code

47781

Product ID

47781-551_9d9e56d5-39d6-61de-dac9-32f1182ccbe0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

felbamate

Dosage form

TABLET

Route

ORAL

Labeler

Alvogen Inc.

Application

ANDA204595

Marketing category

ANDA

Marketing start

2016-12-28

Marketing end

2020-09-01

Substance

FELBAMATE

Active strength

600 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record