# Eulexin

NDC: 80725-143
Generic name: Flutamide
Labeler / Manufacturer: Waylis Therapeutics LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20211112

FDA application: ANDA075298

## Active ingredients

- FLUTAMIDE: 125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80725-143"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80725-143
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0a905e25-42b6-4937-a689-f01a8f22e644