NDC 23155-862 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC23155-862

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 21, 2024
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
23155-862-01100 TABLET in 1 BOTTLE (23155-862-01)Feb 21, 2024
23155-862-0330 TABLET in 1 BOTTLE (23155-862-03)Feb 21, 2024
23155-862-05500 TABLET in 1 BOTTLE (23155-862-05)Feb 21, 2024
23155-862-0990 TABLET in 1 BOTTLE (23155-862-09)Feb 21, 2024

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