NDC 72974-415 – Myfembree

Relugolix 40 mg/1; Estradiol Hemihydrate 1 mg/1; Norethindrone Acetate .5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72974-415

Product details

Brand name
Myfembree
Generic name
Relugolix, estradiol hemihydrate, and norethindrone acetate
Labeler
Sumitomo Pharma America, Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA214846
Marketed since
May 26, 2021
Listing expires
December 31, 2026
Pharmacologic class
Estrogen; Gonadotropin Releasing Hormone Receptor Antagonist; Progestin

Active ingredients

Uses, dosage, side effects and warnings for Myfembree →

Package NDC codes (2)

Package NDCDescriptionSince
72974-415-0128 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72974-415-01)May 26, 2021
72974-415-997 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72974-415-99)Jul 7, 2021