MENOPUR

This brand name is authorized in Austria, Australia, Canada, Cyprus, Ecuador, Estonia, Finland, France, Croatia, Ireland, Israel, Malta, Netherlands, New Zealand, Poland, Romania, Tunisia, Turkey, United Kingdom, South Africa

Active ingredients

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

1 Urofollitropin
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 about Urofollitropin
2 Lutropin alfa
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 about Lutropin alfa
3 Menotropin
UNII 5Y9QQM372Q - MENOTROPINS
Read about Menotropin

Medicine classification

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

ATC code Group title 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)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 2036E, 2038G
Country: CA Health Products and Food Branch Identifier(s): 02283093
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 2218-MEE-0616, 28853-05-09
Country: EE Ravimiamet Identifier(s): 1872895, 1872907, 1872929, 1872930
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 002875, 002892, 087229, 087240
Country: FR Base de données publique des médicaments Identifier(s): 62538194, 66192829
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 193492, 193495, 217077, 48569
Country: IE Health Products Regulatory Authority Identifier(s): 88396, 88397, 88398, 89055
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 4419, 7023, 7024
Country: MT Medicines Authority Identifier(s): MA1314/00701, MA1314/00702, MA1314/00703
Country: NL Z-Index G-Standaard Identifier(s): 16079612
Country: NL Z-Index G-Standaard, PRK Identifier(s): 128627, 57312
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 12914, 19171, 19172
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100112368, 100234597, 100234640, 100332220, 100381364
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W53997001, W53997002, W60840001, W60841001, W69055001, W69056001
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 5523031
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8697621790018, 8697621790476, 8697621790483, 8697621790612, 8697621790629, 8697621790667, 8697621790704
Country: ZA Health Products Regulatory Authority Identifier(s): 44/21.10/0382, 44/21.10/0383, A39/21.10/0357

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