LUVERIS

This brand name is authorized in Austria, Australia, Brazil, Canada, Cyprus, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, United Kingdom, South Africa

Active ingredients

The drug LUVERIS contains one active pharmaceutical ingredient (API):

1 Lutropin alfa
UNII 3JGY52XJNA - LUTROPIN ALFA

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

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
LUVERIS Powder and solvent for solution for injection European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
G03G Gonadotropins and other ovulation stimulants G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system
Discover more medicines within G03G
G03GA07 Lutropin alfa 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 G03GA07

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): 10465T
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 525421001159413
Country: CA Health Products and Food Branch Identifier(s): 02269066
Country: EE Ravimiamet Identifier(s): 1046810, 1046821, 1046832
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 00155006
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 100305
Country: FR Base de données publique des médicaments Identifier(s): 66457697
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 45782
Country: HK Department of Health Drug Office Identifier(s): 49706
Country: IE Health Products Regulatory Authority Identifier(s): 88440, 89083
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 6539
Country: IT Agenzia del Farmaco Identifier(s): 034951018, 034951020, 034951032, 034951044, 034951057, 034951069, 034951071
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1007415, 1008540, 1008541, 1029640, 1029641, 1029663
Country: NL Z-Index G-Standaard Identifier(s): 14661098
Country: NL Z-Index G-Standaard, PRK Identifier(s): 59099
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 10687
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100113238
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W65137001, W65137002, W65137003, W65137004, W65137005, W65137006
Country: SG Health Sciences Authority Identifier(s): 12507P
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 22073021
Country: ZA Health Products Regulatory Authority Identifier(s): 37/21.10/0560

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