Modafinil

Product NDC

62332-106

11-digit product format

623320106

Labeler code

62332

Product ID

62332-106_57c29bec-d763-415e-8ee6-907662200ccf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Modafinil

Dosage form

TABLET

Route

ORAL

Labeler

Alembic Pharmaceuticals Inc.

Application

ANDA202700

Marketing category

ANDA

Marketing start

2016-05-20

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]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record