NDC 71335-2501 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-2501

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207196
Marketed since
February 21, 2024
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
71335-2501-0100 TABLET in 1 BOTTLE, PLASTIC (71335-2501-0)Sep 23, 2024
71335-2501-130 TABLET in 1 BOTTLE, PLASTIC (71335-2501-1)Sep 23, 2024
71335-2501-218 TABLET in 1 BOTTLE, PLASTIC (71335-2501-2)Sep 23, 2024
71335-2501-316 TABLET in 1 BOTTLE, PLASTIC (71335-2501-3)Sep 23, 2024
71335-2501-48 TABLET in 1 BOTTLE, PLASTIC (71335-2501-4)Sep 23, 2024
71335-2501-510 TABLET in 1 BOTTLE, PLASTIC (71335-2501-5)Sep 23, 2024
71335-2501-660 TABLET in 1 BOTTLE, PLASTIC (71335-2501-6)Sep 23, 2024
71335-2501-790 TABLET in 1 BOTTLE, PLASTIC (71335-2501-7)Sep 23, 2024
71335-2501-845 TABLET in 1 BOTTLE, PLASTIC (71335-2501-8)Sep 23, 2024
71335-2501-9180 TABLET in 1 BOTTLE, PLASTIC (71335-2501-9)Sep 23, 2024

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