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
- 71610-991_4c9c4e6a-a290-ada0-e063-6394a90ae619
- Product NDC
- 71610-991
- Form
- TABLET
- Composition / generic term
- Modafinil
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170914
- Source listing expiry
- 20271231
Source-listed ingredients
- MODAFINIL — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71610-991-30) · 71610-991-30
- 60 TABLET in 1 BOTTLE (71610-991-53) · 71610-991-53
- 90 TABLET in 1 BOTTLE (71610-991-60) · 71610-991-60
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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