NDC 87063-306 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC87063-306

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
ASCLEMED USA INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202566
Marketed since
September 27, 2012
Listing expires
December 31, 2027
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (4)

Package NDCDescriptionSince
87063-306-01100 TABLET in 1 BOTTLE (87063-306-01)Sep 10, 2026
87063-306-3030 TABLET in 1 BOTTLE (87063-306-30)Sep 10, 2026
87063-306-6060 TABLET in 1 BOTTLE (87063-306-60)Sep 10, 2026
87063-306-9090 TABLET in 1 BOTTLE (87063-306-90)Sep 10, 2026

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