NDC 71335-1173 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1173

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 (10)

Package NDCDescriptionSince
71335-1173-0100 TABLET in 1 BOTTLE (71335-1173-0)Jul 9, 2024
71335-1173-130 TABLET in 1 BOTTLE (71335-1173-1)Apr 2, 2019
71335-1173-218 TABLET in 1 BOTTLE (71335-1173-2)Jul 9, 2024
71335-1173-316 TABLET in 1 BOTTLE (71335-1173-3)Jul 9, 2024
71335-1173-48 TABLET in 1 BOTTLE (71335-1173-4)Jul 9, 2024
71335-1173-510 TABLET in 1 BOTTLE (71335-1173-5)Jul 9, 2024
71335-1173-660 TABLET in 1 BOTTLE (71335-1173-6)Jun 5, 2019
71335-1173-790 TABLET in 1 BOTTLE (71335-1173-7)Jul 9, 2024
71335-1173-845 TABLET in 1 BOTTLE (71335-1173-8)Jul 9, 2024
71335-1173-9180 TABLET in 1 BOTTLE (71335-1173-9)Jul 9, 2024

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