# Provigil

NDC: 60505-4852
Generic name: Modafinil
Labeler / Manufacturer: Apotex Corp
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250831

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:"60505-4852"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-4852
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0391f182-1958-9fef-a944-53b229ce99e7