United States · FDA National Drug Code directory

Modafinil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
60505-2527_e96ded7a-6c39-63d4-2029-f6db4dc3cd32
Product NDC
60505-2527
Form
TABLET
Composition / generic term
modafinil
Labeler
Apotex Corp.
Marketing category
ANDA
Marketing start / end (source format)
20140203 / 20280731

Source-listed ingredients

  • MODAFINIL — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (60505-2527-1) · 60505-2527-1
  • 30 TABLET in 1 BOTTLE (60505-2527-3) · 60505-2527-3

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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