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Myfembree

NDC 72974-415 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namerelugolix, estradiol hemihydrate, and norethindrone acetate
Labeler / ManufacturerSumitomo Pharma America, Inc
Marketing categoryNew Drug Application (innovator) · App NDA214846
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsESTRADIOL HEMIHYDRATE (1 mg/1)
NORETHINDRONE ACETATE (.5 mg/1)
RELUGOLIX (40 mg/1)
Marketing started20210526
Package count2

External sources

Source: openFDA. Public-domain (CC0).