# Modafinil

NDC: 51407-928
Generic name: modafinil
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140203
Marketing ended: 20271231
FDA application: ANDA077667

## Active ingredients

- MODAFINIL: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51407-928"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-928
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d4c6858-5b2f-f216-e063-6394a90aad5d