# Provigil

NDC: 63459-201
Generic name: Modafinil
Labeler / Manufacturer: Cephalon, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19990215
Marketing ended: 20270831
FDA application: NDA020717

## Active ingredients

- MODAFINIL: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63459-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63459-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e16c26ad-7bc2-d155-3a5d-da83ad6492c8