This brand name is authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Germany, Hong Kong SAR China, Ireland, Israel, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Tunisia, Turkey, UK.
The drug ACLASTA contains one active pharmaceutical ingredient (API):
1
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UNII
6XC1PAD3KF - ZOLEDRONIC ACID
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Zoledronic acid belongs to the class of bisphosphonates and acts primarily on bone. It is an inhibitor of osteoclastic bone resorption. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| M05BA08 | Zoledronic acid | M Musculo-skeletal system → M05 Drugs for treatment of bone diseases → M05B Drugs affecting bone structure and mineralization → M05BA Bisphosphonates |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 9288W, 9350D |
| BR | Câmara de Regulação do Mercado de Medicamentos | 526526701159419 |
| CA | Health Products and Food Branch | 02269198 |
| DE | Bundesinstitut für Arzneimittel und Medizinprodukte | 00693807, 04392020, 04944241, 05006970, 05453930, 09166943, 09643596, 10068306, 10227874, 10857693, 11030004, 11100503, 11157377, 11874363, 12340787, 12457880, 14357102, 14367425, 15382148, 15434170 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 4469-MEE-1118 |
| EE | Ravimiamet | 1201712, 1265666 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 418386 |
| FR | Base de données publique des médicaments | 67306342 |
| GB | Medicines & Healthcare Products Regulatory Agency | 104230, 392262 |
| HK | Department of Health Drug Office | 54084, 66154 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6016 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1005667, 1026398 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 051M2006 |
| NL | Z-Index G-Standaard, PRK | 79790 |
| NZ | Medicines and Medical Devices Safety Authority | 11849 |
| PL | Rejestru Produktów Leczniczych | 100137948 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W64472001, W64472002 |
| SG | Health Sciences Authority | 13192P |
| TN | Direction de la Pharmacie et du Médicament | 10283281 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699504690019 |
| ZA | Health Products Regulatory Authority | A39/34/0575 |
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