NDC 68788-8653 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68788-8653

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207196
Marketed since
May 9, 2024
Listing expires
December 31, 2027
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (3)

Package NDCDescriptionSince
68788-8653-330 TABLET in 1 BOTTLE (68788-8653-3)May 9, 2024
68788-8653-660 TABLET in 1 BOTTLE (68788-8653-6)May 9, 2024
68788-8653-990 TABLET in 1 BOTTLE (68788-8653-9)May 9, 2024

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