Modafinil

Product NDC

71335-0259

11-digit product format

713350259

Labeler code

71335

Product ID

71335-0259_638ef321-5d4e-47bf-91e6-1a4e30c0bfb8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

modafinil

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077667

Marketing category

ANDA

Marketing start

2014-02-03

Marketing end

0000-00-00

Substance

MODAFINIL

Active strength

200 mg/1

Pharmacologic classes

Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record