NDC 23155-604 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC23155-604

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207196
Marketed since
February 18, 2021
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
23155-604-01100 TABLET in 1 BOTTLE, PLASTIC (23155-604-01)Feb 18, 2021
23155-604-0330 TABLET in 1 BOTTLE, PLASTIC (23155-604-03)Feb 18, 2021
23155-604-05500 TABLET in 1 BOTTLE, PLASTIC (23155-604-05)Feb 18, 2021
23155-604-0990 TABLET in 1 BOTTLE, PLASTIC (23155-604-09)Feb 18, 2021

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