NDC 50268-571 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC50268-571

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202566
Marketed since
August 1, 2016
Listing expires
December 31, 2027
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (1)

Package NDCDescriptionSince
50268-571-1220 BLISTER PACK in 1 BOX (50268-571-12) / 1 TABLET in 1 BLISTER PACK (50268-571-11)Aug 1, 2016

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