NDC 71610-685 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71610-685

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077667
Marketed since
February 3, 2014
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (2)

Package NDCDescriptionSince
71610-685-3030 TABLET in 1 BOTTLE (71610-685-30)Jan 11, 2023
71610-685-5360 TABLET in 1 BOTTLE (71610-685-53)Jan 11, 2023

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