NDC 72974-415

Myfembree

Relugolix, Estradiol Hemihydrate, And Norethindrone Acetate

Myfembree is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Myovant Sciences, Inc.. The primary component is Relugolix; Estradiol Hemihydrate; Norethindrone Acetate.

Product ID72974-415_4d145097-231a-4d89-ae96-f3e86752bf7c
NDC72974-415
Product TypeHuman Prescription Drug
Proprietary NameMyfembree
Generic NameRelugolix, Estradiol Hemihydrate, And Norethindrone Acetate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2021-05-26
Marketing CategoryNDA /
Application NumberNDA214846
Labeler NameMyovant Sciences, Inc.
Substance NameRELUGOLIX; ESTRADIOL HEMIHYDRATE; NORETHINDRONE ACETATE
Active Ingredient Strength40 mg/1; mg/1; mg/1
Pharm ClassesEstradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [CS],Progestin [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 72974-415-01

28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72974-415-01)
Marketing Start Date2021-05-26
NDC Exclude FlagN
Sample Package?N

Drug Details


Trademark Results [Myfembree]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MYFEMBREE
MYFEMBREE
90593915 not registered Live/Pending
Myovant Sciences GmbH
2021-03-22
MYFEMBREE
MYFEMBREE
88768680 not registered Live/Pending
Myovant Sciences GmbH
2020-01-22

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