NDC 57237-154 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC57237-154

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Rising Pharma Holdings, 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 (3)

Package NDCDescriptionSince
57237-154-01100 TABLET in 1 BOTTLE (57237-154-01)Sep 27, 2012
57237-154-3030 TABLET in 1 BOTTLE (57237-154-30)Sep 27, 2012
57237-154-9090 TABLET in 1 BOTTLE (57237-154-90)Sep 27, 2012

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