NDC 71335-1122 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1122

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Bryant Ranch Prepack
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 (7)

Package NDCDescriptionSince
71335-1122-130 TABLET in 1 BOTTLE (71335-1122-1)Feb 26, 2019
71335-1122-260 TABLET in 1 BOTTLE (71335-1122-2)Mar 14, 2019
71335-1122-328 TABLET in 1 BOTTLE (71335-1122-3)Mar 14, 2019
71335-1122-490 TABLET in 1 BOTTLE (71335-1122-4)Mar 14, 2019
71335-1122-545 TABLET in 1 BOTTLE (71335-1122-5)Jul 9, 2024
71335-1122-6180 TABLET in 1 BOTTLE (71335-1122-6)Jul 9, 2024
71335-1122-7100 TABLET in 1 BOTTLE (71335-1122-7)Dec 12, 2022

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