NDC 55253-802 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC55253-802

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
CIMA LABS INC.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA020717
Marketed since
March 29, 2012
Marketing end
February 28, 2027
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (1)

Package NDCDescriptionSince
55253-802-9090 TABLET in 1 BOTTLE (55253-802-90)Mar 29, 2012

Other Modafinil products