NDC 71335-2258 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-2258

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207196
Marketed since
February 18, 2021
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
71335-2258-0100 TABLET in 1 BOTTLE (71335-2258-0)Apr 3, 2024
71335-2258-130 TABLET in 1 BOTTLE (71335-2258-1)Nov 2, 2023
71335-2258-218 TABLET in 1 BOTTLE (71335-2258-2)Apr 3, 2024
71335-2258-316 TABLET in 1 BOTTLE (71335-2258-3)Apr 3, 2024
71335-2258-48 TABLET in 1 BOTTLE (71335-2258-4)Apr 3, 2024
71335-2258-510 TABLET in 1 BOTTLE (71335-2258-5)Apr 3, 2024
71335-2258-660 TABLET in 1 BOTTLE (71335-2258-6)Oct 26, 2023
71335-2258-790 TABLET in 1 BOTTLE (71335-2258-7)Apr 3, 2024
71335-2258-845 TABLET in 1 BOTTLE (71335-2258-8)Apr 3, 2024
71335-2258-9180 TABLET in 1 BOTTLE (71335-2258-9)Apr 3, 2024

Other Modafinil products