NDC 71610-976 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71610-976

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209966
Marketed since
February 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (3)

Package NDCDescriptionSince
71610-976-3030 TABLET in 1 BOTTLE (71610-976-30)Dec 17, 2025
71610-976-5360 TABLET in 1 BOTTLE (71610-976-53)Dec 17, 2025
71610-976-6090 TABLET in 1 BOTTLE (71610-976-60)Dec 17, 2025

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