NDC 72578-006 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC72578-006

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Viona Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209966
Marketed since
February 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (3)

Package NDCDescriptionSince
72578-006-01100 TABLET in 1 BOTTLE (72578-006-01)Feb 15, 2019
72578-006-0630 TABLET in 1 BOTTLE (72578-006-06)Feb 15, 2019
72578-006-1690 TABLET in 1 BOTTLE (72578-006-16)Feb 15, 2019

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