OVALEAP

This brand name is authorized in Austria, Estonia, Spain, Finland, France, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom

Active ingredients

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

1 Follitropin alfa
UNII 076WHW89TW - FOLLITROPIN

In women, the most important effect resulting from parenteral administration of FSH is the development of mature Graafian follicles.

Read about Follitropin alfa

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
OVALEAP 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
G03GA05 Follitropin 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 G03GA05

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1628636, 1628647, 1628658
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 113871001, 113871002, 113871003
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 455692, 584262, 594538
Country: FR Base de données publique des médicaments Identifier(s): 67050131, 67945023, 68787170
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 311771, 311774, 311777
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8024, 8025, 8026
Country: IT Agenzia del Farmaco Identifier(s): 043029014, 043029026, 043029038
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1071579, 1071580, 1071581
Country: NL Z-Index G-Standaard, PRK Identifier(s): 129410, 129429, 129658
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100304458, 100304464, 100304470
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W65720001, W65721001, W65722001

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