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
- 43353-925_01f751d9-8907-4a54-b2e9-f57a8f150920
- Product NDC
- 43353-925
- Form
- TABLET
- Composition / generic term
- modafinil
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20120329
- Source listing expiry
- 20261231
Source-listed ingredients
- MODAFINIL — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (43353-925-30) · 43353-925-30
- 60 TABLET in 1 BOTTLE, PLASTIC (43353-925-53) · 43353-925-53
Source and coverage
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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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