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
- 63629-7315_30de185f-afb7-4999-8903-27eed51ad246
- Product NDC
- 63629-7315
- Form
- TABLET
- Composition / generic term
- Modafinil
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120927
- Source listing expiry
- 20261231
Source-listed ingredients
- MODAFINIL — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (63629-7315-0) · 63629-7315-0
- 30 TABLET in 1 BOTTLE (63629-7315-1) · 63629-7315-1
- 18 TABLET in 1 BOTTLE (63629-7315-2) · 63629-7315-2
- 16 TABLET in 1 BOTTLE (63629-7315-3) · 63629-7315-3
- 8 TABLET in 1 BOTTLE (63629-7315-4) · 63629-7315-4
- 10 TABLET in 1 BOTTLE (63629-7315-5) · 63629-7315-5
- 60 TABLET in 1 BOTTLE (63629-7315-6) · 63629-7315-6
- 90 TABLET in 1 BOTTLE (63629-7315-7) · 63629-7315-7
- 45 TABLET in 1 BOTTLE (63629-7315-8) · 63629-7315-8
- 180 TABLET in 1 BOTTLE (63629-7315-9) · 63629-7315-9
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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