NDC 71205-477 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71205-477

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202566
Marketed since
September 27, 2012
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
71205-477-3030 TABLET in 1 BOTTLE (71205-477-30)Sep 29, 2020
71205-477-6060 TABLET in 1 BOTTLE (71205-477-60)Sep 29, 2020
71205-477-9090 TABLET in 1 BOTTLE (71205-477-90)Sep 29, 2020

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