MERIOFERT

This brand name is authorized in Austria, Cyprus, Ecuador, Estonia, Lithuania, Malta, Netherlands, Romania, Spain, Turkey, UK.

Active ingredients

The drug MERIOFERT contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 58G97EP42I - FOLLICLE-STIMULATING HORMONE (HUMAN CLONE .LAMBDA.15B .BETA.-SUBUNIT PROTEIN MOIETY REDUCED)
 

Urofollitropin contains a highly purified preparation of urinary FSH extracted from the urine of postmenopausal women. FSH stimulates ovarian follicular growth and development as well as gonadal steroid production in women who do not have primary ovarian failure.

 
Read more about Urofollitropin
2
UNII 8XA4VN1LH4 - LUTEINIZING HORMONE
 

Lutropin alfa is a recombinant human Luteinising Hormone (r-hLH). Luteinising Hormone (LH) binds on the ovarian theca (and granulosa) cells and testicular Leydig cells, to a receptor shared with human chorionic gonadotropin hormone (hCG). Lutropin alfa in association with a Follicle Stimulating Hormone (FSH) preparation is recommended for the stimulation of follicular development in adult women with severe Luteinising Hormone (LH) and FSH deficiency.

 
Read more about Lutropin alfa

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
G03GA02 Human menopausal gonadotrophin G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03G Gonadotropins and other ovulation stimulants → G03GA Gonadotropins
Discover more medicines within G03GA02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 7140-MEE-0322, 7156-MEE-0322
EE Ravimiamet 1823059, 1823060, 1823071, 1823082, 1823093, 1823105
ES Centro de información online de medicamentos de la AEMPS 79761, 79762
GB Medicines & Healthcare Products Regulatory Agency 347368, 347371
LT Valstybinė vaistų kontrolės tarnyba 1091920, 1091921, 1091922, 1091923, 1091924, 1091925
MT Medicines Authority AA770/08501, AA770/08502
NL Z-Index G-Standaard, PRK 128627, 57312
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64576001, W64576002, W64576003, W64577001, W64577002, W64577003, W64578001, W64578002, W64578003, W64579001, W64579002, W64579003, W69384001
TR İlaç ve Tıbbi Cihaz Kurumu 8680426040037, 8680426040044

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.