NDC 65862-601 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC65862-601

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Aurobindo Pharma Limited
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 (4)

Package NDCDescriptionSince
65862-601-01100 TABLET in 1 BOTTLE (65862-601-01)Sep 27, 2012
65862-601-3030 TABLET in 1 BOTTLE (65862-601-30)Sep 27, 2012
65862-601-9090 TABLET in 1 BOTTLE (65862-601-90)Sep 27, 2012
65862-601-991000 TABLET in 1 BOTTLE (65862-601-99)Sep 27, 2012

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