MERIONAL

This brand name is authorized in Ecuador, Estonia, South Africa, Tunisia.

Active ingredients

The drug MERIONAL 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
G03GA30 Combinations 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 G03GA30

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 22.478-1-01-06, 22.501-1-01-06
EE Ravimiamet 1628704
TN Direction de la Pharmacie et du Médicament 13533021, 13533022
ZA Health Products Regulatory Authority 48/21.10/0402

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