# YONSA

NDC: 47335-401
Generic name: abiraterone acetate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180522

FDA application: NDA210308

## Active ingredients

- ABIRATERONE ACETATE: 125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-401"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-401
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b8967e10-f768-47ce-ac9e-2324c8390132