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
- 23155-604_539210d2-638a-4fd5-a934-d7b5fac982e4
- Product NDC
- 23155-604
- Form
- TABLET
- Composition / generic term
- Modafinil
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210218
- Source listing expiry
- 20271231
Source-listed ingredients
- MODAFINIL — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (23155-604-01) · 23155-604-01
- 30 TABLET in 1 BOTTLE, PLASTIC (23155-604-03) · 23155-604-03
- 500 TABLET in 1 BOTTLE, PLASTIC (23155-604-05) · 23155-604-05
- 90 TABLET in 1 BOTTLE, PLASTIC (23155-604-09) · 23155-604-09
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.
Browse United States records →