This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, South Africa, Spain, Tunisia, Turkey, UK.
The drug CUROSURF contains one active pharmaceutical ingredient (API):
1
|
UNII
KE3U2023NP - PORACTANT ALFA
|
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| R07AA02 | Natural phospholipids | R Respiratory system → R07 Other respiratory system products → R07A Other respiratory system products → R07AA Lung surfactants |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 508501201154414, 508501202150412 |
| CA | Health Products and Food Branch | 02241551 |
| EE | Ravimiamet | 1029732, 1077993, 1377121 |
| ES | Centro de información online de medicamentos de la AEMPS | 59600, 59601 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 107002, 571181 |
| FR | Base de données publique des médicaments | 60301200, 64447081 |
| GB | Medicines & Healthcare Products Regulatory Agency | 80094, 80097 |
| HK | Department of Health Drug Office | 54928, 54929 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-666938777 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6994, 8686 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1010206, 1069246 |
| MT | Medicines Authority | MA173/00104, MA173/00105, PI565/01003A |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 539M2004 |
| NL | Z-Index G-Standaard, PRK | 72109, 72117 |
| NZ | Medicines and Medical Devices Safety Authority | 10932 |
| PL | Rejestru Produktów Leczniczych | 100080869, 100417369 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W08909001 |
| TN | Direction de la Pharmacie et du Médicament | 7133081H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699822770028, 8699822770035 |
| US | FDA, National Drug Code | 10122-510 |
| ZA | Health Products Regulatory Authority | 33/10.2.2/0528 |
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