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FDA approval · 2024-04-30

FDA Approved: MYFEMBREE — Supplemental Application (Sumitomo Pharma America, Inc)

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Summary

FDA approved a supplemental application for MYFEMBREE, a relugolix/estradiol hemihydrate/norethindrone acetate combination, expanding its labeling or indication…

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Diseases / indications

Drugs mentioned

  • MYFEMBREE (relugolix, estradiol hemihydrate, and norethindrone acetate)

Snippet

SUPPL AP for MYFEMBREE (RELUGOLIX, ESTRADIOL HEMIHYDRATE, AND NORETHINDRONE ACETATE)