# Abiraterone acetate

NDC: 71921-177
Generic name: Abiraterone acetate
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230410

FDA application: ANDA215086

## Active ingredients

- ABIRATERONE ACETATE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-177"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-177
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=68121a71-5024-4f9e-bd9c-2d412f6a6355