# Armodafinil

NDC: 69339-178
Generic name: Armodafinil
Labeler / Manufacturer: Natco Pharma USA LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230323

FDA application: ANDA202768

## Active ingredients

- ARMODAFINIL: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69339-178"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69339-178
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de2f0921-e791-426c-9192-2b7162e2158c