Lutetium Oxodotreotide
Records for this ingredient, by country (identity only).
ATC — · 5 markets · 7 records
AU 2 records · 1 shown of 1
- 370 MBq/mL per mL / per unit basis not statedinjectionLUTATHERA lutetium (177Lu) oxodotreotide 370 MBq/mL solution for intravenous infusion vial
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
HK 2 records · 0 shown of 0
2 records · 0 manufacturers 2 registros · 0 fabricantes 2 个记录 · 0 个厂家 2 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
SG 1 records · 1 shown of 1
- 370 MBq/mL per mL / per unit basis not statedinjectionLUTATHERA SOLUTION FOR INFUSION 370 MBQ/ML
JP 1 records · 1 shown of 1
- 7400 mg per mL / per unit basis not statedinjectionルタテラ静注
EU 1 records · 0 shown of 0
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
Some strengths are recorded without a per mL / per unit basis. They are shown as recorded and are not compared with other markets.
| Strength / form / release | AU | SG | HK | JP | EU |
|---|---|---|---|---|---|
| 370 MBq/mL per mL / per unit basis not stated cannot compare injection | LUTATHERA lutetium (177Lu) oxodotreotide 370 MBq/mL solution for intravenous infusion vial | LUTATHERA SOLUTION FOR INFUSION 370 MBQ/ML | |||
| 7400 mgRecorded as: 7.4 g per mL / per unit basis not stated cannot compare injection | ルタテラ静注 | ||||
unknown | Lutathera | LUTATHERA SOLUTION FOR INFUSION 370MBQ/ML | Lutathera |
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Each country column shows the locally registered trade names — not translations.
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Hong Kong records are name/ingredient-level only: no strength, dosage form or registration status; on the register does not prove current supply.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.