Sebelipase Alfa
ATC A16AB14 · 7 markets · 8 records
AU 2 records · 1 shown of 1
- 2 mg/mLinjectionKANUMA sebelipase alfa rce 2 mg/mL injection 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
GB 1 records · 1 shown of 1
- 20 mg/10 mLinjectionKanuma 20mg/10ml concentrate for solution for infusion vials
CA 1 records · 1 shown of 1
- 2 mgliquidKANUMA
SG 1 records · 1 shown of 1
- 2 mg/mLinjectionKANUMA CONCENTRATE FOR SOLUTION FOR INFUSION 2 MG/ML
HK 1 records · 0 shown of 0
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
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
FR 1 records · 1 shown of 1
- 2 mg/1 mLinjectionKANUMA 2 mg/ml,solution à diluer pour perfusion
| Strength / form / release | GB | CA | AU | SG | HK | EU | FR |
|---|---|---|---|---|---|---|---|
| 2 mg/mL injection | KANUMA sebelipase alfa rce 2 mg/mL injection intravenous infusion vial | KANUMA CONCENTRATE FOR SOLUTION FOR INFUSION 2 MG/ML | |||||
| 2 mg liquid | KANUMA | ||||||
| 20 mg/10 mL injection | Kanuma 20mg/10ml concentrate for solution for infusion vials | ||||||
| 2 mg/1 mL injection | KANUMA 2 mg/ml,solution à diluer pour perfusion | ||||||
unknown | KANUMA | KANUMA CONCENTRATE FOR SOLUTION FOR INFUSION 20MG/10ML | KANUMA |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in GB and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en GB que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 GB 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 GB 有記錄(未在本表顯示)。
“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.