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FDA approval · 2022-01-28

FDA Approved: YONSA — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

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Summary

The FDA approved a supplemental application for YONSA (abiraterone acetate) submitted by Sun Pharmaceutical Industries, Inc. under NDA 210308.

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Diseases / indications

Drugs mentioned

  • YONSA (abiraterone acetate)

Snippet

SUPPL AP for YONSA (ABIRATERONE ACETATE)