# Modafinil

NDC: 69452-342
Generic name: Modafinil
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220228

FDA application: ANDA078963

## 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:"69452-342"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-342
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63604fef-0b80-40ce-8dbf-3384f1aee395