NDC 68071-5121 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68071-5121

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
NuCare Pharmaceuticals,Inc.
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 (1)

Package NDCDescriptionSince
68071-5121-330 TABLET in 1 BOTTLE (68071-5121-3)Dec 4, 2019

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