This brand name is authorized in Australia, Austria, Brazil, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, UK.
The drug FERINJECT contains one active pharmaceutical ingredient (API):
1
|
UNII
02414N8GQC - DEXTRIFERRON
|
Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| FERINJECT Solution for injection/infusion | 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 | |
|---|---|---|
| B03AB05 | Ferric oxide polymaltose complexes | B Blood and blood forming organs → B03 Antianemic preparations → B03A Iron preparations → B03AB Iron trivalent, oral preparations |
| B03AC | Iron trivalent, parenteral preparations | B Blood and blood forming organs → B03 Antianemic preparations → B03A Iron preparations |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 10104T, 11702X |
| BR | Câmara de Regulação do Mercado de Medicamentos | 501113010020402 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 1867-MEE-0316 |
| EE | Ravimiamet | 1236934, 1236945, 1387795, 1387807, 1548233, 1548244, 1671500, 1862535 |
| ES | Centro de información online de medicamentos de la AEMPS | 69771 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 145795, 145817, 400244 |
| FR | Base de données publique des médicaments | 60960624 |
| GB | Medicines & Healthcare Products Regulatory Agency | 137526, 137529, 243929 |
| HK | Department of Health Drug Office | 64137, 64138 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-646532651 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6674 |
| JP | 医薬品医療機器総合機構 | 3222404A1021 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1022620, 1022621, 1035297, 1035298, 1062875, 1062876, 1072065 |
| NL | Z-Index G-Standaard | 15467112 |
| NL | Z-Index G-Standaard, PRK | 115088, 89230, 89249 |
| NZ | Medicines and Medical Devices Safety Authority | 15189 |
| PL | Rejestru Produktów Leczniczych | 100220253 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W59531001, W59531002, W59531003, W59531004, W59531005, W59531006 |
| SG | Health Sciences Authority | 14035P |
| TN | Direction de la Pharmacie et du Médicament | 6653701H |
| ZA | Health Products Regulatory Authority | 45/8.3/0948 |
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