NDC 71610-991 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71610-991

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
September 14, 2017
Listing expires
December 31, 2027
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (3)

Package NDCDescriptionSince
71610-991-3030 TABLET in 1 BOTTLE (71610-991-30)Mar 9, 2026
71610-991-5360 TABLET in 1 BOTTLE (71610-991-53)Mar 9, 2026
71610-991-6090 TABLET in 1 BOTTLE (71610-991-60)Mar 9, 2026

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