This brand name is authorized in United States. It is also authorized in Australia, Brazil, Canada, Croatia, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Mexico, Netherlands, New Zealand, Nigeria, Poland, Romania, Singapore, South Africa, Spain, Turkey, UK.
The drug CRINONE contains one active pharmaceutical ingredient (API):
1
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UNII
4G7DS2Q64Y - PROGESTERONE
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Progesterone is a natural progestogen, the main hormone of the corpus luteum and the placenta. It acts on the endometrium by converting the proliferating phase to the secretory phase. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| CRINONE Vaginal gel | 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 | |
|---|---|---|
| G03DA04 | Progesterone | G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03D Progestogens → G03DA Pregnen (4) derivatives |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 6366C |
| BR | Câmara de Regulação do Mercado de Medicamentos | 525421601164310, 525421602160319 |
| CA | Health Products and Food Branch | 02241013 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 2385-MEE-0816 |
| EE | Ravimiamet | 1134548, 1634846, 1634857, 1765919, 1765920 |
| ES | Centro de información online de medicamentos de la AEMPS | 62915 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 053843 |
| FR | Base de données publique des médicaments | 65015968 |
| GB | Medicines & Healthcare Products Regulatory Agency | 42123 |
| HK | Department of Health Drug Office | 44527 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-302863360 |
| IE | Health Products Regulatory Authority | 18927, 18928, 36553, 54352 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6538 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1072219, 1076147, 1093375 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 303M97 |
| NG | Registered Drug Product Database | C4-1804 |
| NL | Z-Index G-Standaard, PRK | 129402 |
| NZ | Medicines and Medical Devices Safety Authority | 10232 |
| PL | Rejestru Produktów Leczniczych | 100339095, 100459097 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W61888001, W61888002 |
| SG | Health Sciences Authority | 10884P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699777342035 |
| US | FDA, National Drug Code | 0023-6150, 0023-6151, 52544-256 |
| ZA | Health Products Regulatory Authority | A38/21.8.2/0615 |
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