MedPath

Menotropins

Generic Name
Menotropins
Brand Names
Menopur
Drug Type
Biotech
CAS Number
9002-68-0
Unique Ingredient Identifier
8FYM5179QJ

Overview

Menotropins contains follicle stimulating hormone (FSH) and luteinizing hormone (LH) purified from the urine of postmenopausal women. It is used as a fertility medication that is injected either subcutaneously or intramuscularly. It is composed of LH with 2 subunits, alpha = 92 residues, beta = 121 residues and FSH with 2 subunits, alpha = 92 residues, beta=111 residues.

Indication

For the treatment of female infertility

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2020/06/04
Not Applicable
Completed
2020/05/12
Phase 4
UNKNOWN
2019/12/10
Not Applicable
Withdrawn
2018/11/09
Not Applicable
Completed
2018/07/06
Not Applicable
Completed
Reproductive & Genetic Hospital of CITIC-Xiangya
2017/06/06
Phase 4
Completed
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology
2016/12/14
Phase 4
UNKNOWN
2016/10/17
N/A
Completed
2016/07/18
N/A
Completed
2016/05/18
Not Applicable
UNKNOWN
Navy General Hospital, Beijing

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
MENOPUR
Ferring Inc
02283093
Powder For Solution - Subcutaneous
75 UNIT / VIAL
9/19/2006
REPRONEX
Ferring Inc
02247790
Powder For Solution - Intramuscular ,  Subcutaneous
75 UNIT / VIAL
8/28/2003

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
MERIOFERT KIT 75 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ibsa Farmaceutici Italia S.R.L.
79762
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Commercialized
MERIOFERT 75 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ibsa Farmaceutici Italia S.R.L.
89199
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Not Commercialized
MENOPUR 600 UI SOLUCION INYECTABLE EN PLUMA PRECARGADA
Ferring S.A.U.
87965
SOLUCIÓN INYECTABLE EN PLUMA PRECARGADA
Diagnóstico Hospitalario
Not Commercialized
MENOPUR 75 UNIDADES INTERNACIONALES POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ferring S.A.
62583
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Not Commercialized
MERIOFERT 150 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ibsa Farmaceutici Italia S.R.L.
89198
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Not Commercialized
MENOPUR 1200 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ferring S.A.
73586
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Commercialized
MENOPUR 1200 UI SOLUCION INYECTABLE EN PLUMA PRECARGADA
Ferring S.A.U.
87966
SOLUCIÓN INYECTABLE EN PLUMA PRECARGADA
Diagnóstico Hospitalario
Not Commercialized
MERIOFERT KIT 900 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ibsa Farmaceutici Italia S.R.L.
88705
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Commercialized
MERIOFERT KIT 150 UI POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Ibsa Farmaceutici Italia S.R.L.
79761
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Diagnóstico Hospitalario
Commercialized
HMG-LEPORI 75 U.I. POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
Angelini Pharma Espana S.L.
55890
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica
Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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