NDC 72974-415
Myfembree 1 mg / 40 mg / 0.5 mg tablet, film coated
On the label: Sumitomo Pharma America, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sumitomo Pharma America, Inc. names for other drugs.
Product details
- Generic drug
- Estradiol and Norethindrone and Relugolix: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 1 mg / 40 mg / 0.5 mg
- Approval
- NDA NDA214846
- On the market since
- May 26, 2021
- Package NDCs
72974-415-0172974-415-99- Official label
- DailyMed (National Library of Medicine), updated Oct 27, 2026
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