FDA
approval
· 2024-04-30
FDA Approved: MYFEMBREE — Supplemental Application (Sumitomo Pharma America, Inc)
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
Snippet
SUPPL AP for MYFEMBREE (RELUGOLIX, ESTRADIOL HEMIHYDRATE, AND NORETHINDRONE ACETATE)