NDC 63629-7315 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC63629-7315

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
63629-7315-0100 TABLET in 1 BOTTLE (63629-7315-0)Jul 8, 2024
63629-7315-130 TABLET in 1 BOTTLE (63629-7315-1)Jun 26, 2017
63629-7315-218 TABLET in 1 BOTTLE (63629-7315-2)Jul 8, 2024
63629-7315-316 TABLET in 1 BOTTLE (63629-7315-3)Jul 8, 2024
63629-7315-48 TABLET in 1 BOTTLE (63629-7315-4)Jul 8, 2024
63629-7315-510 TABLET in 1 BOTTLE (63629-7315-5)Jul 8, 2024
63629-7315-660 TABLET in 1 BOTTLE (63629-7315-6)Oct 18, 2018
63629-7315-790 TABLET in 1 BOTTLE (63629-7315-7)Jul 8, 2024
63629-7315-845 TABLET in 1 BOTTLE (63629-7315-8)Jul 8, 2024
63629-7315-9180 TABLET in 1 BOTTLE (63629-7315-9)Jul 8, 2024

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