This brand name is authorized in United States. It is also authorized in Australia, Brazil, Canada, Ecuador, Estonia, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Mexico, Netherlands, New Zealand, Nigeria, Poland, Singapore, South Africa, Turkey, UK.
The drug DEPO-PROVERA contains one active pharmaceutical ingredient (API):
1
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UNII
C2QI4IOI2G - MEDROXYPROGESTERONE ACETATE
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Medroxyprogesterone acetate exerts anti-oestrogenic, anti-androgenic and antigonadotrophic effects. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| DEPO-PROVERA Suspension for injection | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| G03AC06 | Medroxyprogesterone | G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AC Progestogens |
| L02AB02 | Medroxyprogesterone | L Antineoplastic and immunomodulating agents → L02 Endocrine therapy → L02A Hormones and related agents → L02AB Progestogens |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 3118D |
| BR | Câmara de Regulação do Mercado de Medicamentos | 522717100060617, 522717100060717, 522718030075303 |
| CA | Health Products and Food Branch | 00585092 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 27.630-1-01-12 |
| EE | Ravimiamet | 1009213, 1063550, 1063561 |
| FR | Base de données publique des médicaments | 62429736 |
| GB | Medicines & Healthcare Products Regulatory Agency | 185727, 19864, 36035 |
| HK | Department of Health Drug Office | 43794 |
| IE | Health Products Regulatory Authority | 55581, 60088 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 3048, 42 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1090585 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 59742 |
| NG | Registered Drug Product Database | 04-2310 |
| NL | Z-Index G-Standaard | 14040387, 14040395 |
| NL | Z-Index G-Standaard, PRK | 67113, 67121 |
| NZ | Medicines and Medical Devices Safety Authority | 292 |
| PL | Rejestru Produktów Leczniczych | 100017902, 100081219, 100257210, 100292956, 100341436 |
| SG | Health Sciences Authority | 04540P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681308771070 |
| US | FDA, National Drug Code | 0009-0626, 0009-0746, 0009-4709, 0009-7376, 50090-0665 |
| ZA | Health Products Regulatory Authority | E/21.8.2/114 |
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