# abiraterone acetate

NDC: 71921-178
Generic name: abiraterone acetate
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220815

FDA application: ANDA212462

## Active ingredients

- ABIRATERONE ACETATE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-178"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-178
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b3e7f851-4132-4003-8f14-0eea21e5009c