NDC 72974-415-99
Myfembree 1 mg/1
relugolix, estradiol hemihydrate, and norethindrone acetate · TABLET, FILM COATED
Myfembree is a tablet, film coated containing relugolix, estradiol hemihydrate, and norethindrone acetate at a strength of 1 mg/1. Manufactured by Sumitomo Pharma America, Inc.
Key Facts
- Brand Name
- Myfembree
- Generic Name
- relugolix, estradiol hemihydrate, and norethindrone acetate
- NDC Code (Package)
72974-415-99- NDC Code (Product)
72974-415- Manufacturer
- Sumitomo Pharma America, Inc
- Strength
- 1 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA214846
- Drug Class
- Gonadotropin Releasing Hormone Receptor Antagonist [EPC]
- Marketing Start
- 05/26/2021
Recall History
No Recall HistoryView Full Drug Page
Myfembree — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.