INTRAROSA

This brand name is authorized in Austria, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Lithuania, Poland, United Kingdom, United States

Active ingredients

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

1 Prasterone
UNII 459AG36T1B - PRASTERONE

Prasterone, i.e. dehydroepiandrosterone (DHEA), biochemically and biologically identical to the endogenous human DHEA, is a precursor steroid which is inactive by itself and it is converted into oestrogens and androgens. Intrarosa is thus different from the oestrogens preparations since it delivers also androgen metabolites.

Read about Prasterone

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
INTRAROSA Pessary 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
A14AA07 Prasterone A Alimentary tract and metabolism → A14 Anabolic agents for systemic use → A14A Anabolic steroids → A14AA Androstan derivatives
Discover more medicines within A14AA07

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): 1765661
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1171255001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 098502
Country: FR Base de données publique des médicaments Identifier(s): 60073960
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 369144
Country: HK Department of Health Drug Office Identifier(s): 66651
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8626
Country: IT Agenzia del Farmaco Identifier(s): 045933013
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1085076
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100402008
Country: US FDA, National Drug Code Identifier(s): 64011-601

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