Armodafinil

Product NDC

51991-322

11-digit product format

519910322

Labeler code

51991

Product ID

51991-322_7b2c30e2-6758-463b-b355-35a9058f1baf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Armodafinil

Dosage form

TABLET

Route

ORAL

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA202768

Marketing category

ANDA

Marketing start

2016-11-28

Marketing end

0000-00-00

Substance

ARMODAFINIL

Active strength

50 mg/1

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record