This brand name is authorized in Austria, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Lithuania, Poland, United Kingdom, United States
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. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
INTRAROSA Pessary | European Medicines Agency (EU) | MPI, EU: SmPC |
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 |
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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