Modafinil

Product NDC

68788-7408

11-digit product format

687887408

Labeler code

68788

Product ID

68788-7408_d7d2d764-200e-4cda-80e3-61be32ca72dd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

modafinil

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA076594

Marketing category

ANDA

Marketing start

2018-06-06

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

2020-12-31

Current FDA listing

Historical FDA.report record