# Abiraterone

NDC: 82009-140
Generic name: Abiraterone acetate
Labeler / Manufacturer: Quallent Pharmaceuticals Health LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191007

FDA application: ANDA210686

## 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:"82009-140"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-140
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f5b628b-69da-4a04-a4d5-623b18d1fd5d