# Modafinil

NDC: 70771-1052
Generic name: Modafinil
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180104

FDA application: ANDA209966

## Active ingredients

- MODAFINIL: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f39820fb-8248-4d42-854c-6fe2d9b92d36