Cerliponase Alfa
Records for this ingredient, by country (identity only).
ATC A16AB17 · 6 markets · 7 records
AU 2 records · 1 shown of 1
- 30 mg/mL per mL / per unit basis not statedinjectionBRINEURA cerliponase alfa (rch) 150 mg/5 mL solution for injection vial with flushing solution 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
- 150 mg/5 mLinjectionBrineura 150mg/5ml solution for infusion vials
CA 1 records · 1 shown of 1
- 30 mg/1 mLliquidBrineura
TW 1 records · 1 shown of 1
- 150 mg per mL / per unit basis not statedinjectionBRINEURA 150 mg solution for infusion倍原力150毫克輸注液
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
- 150 mg/5 mLinjectionBRINEURA 150 mg, solution pour perfusion
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 | GB | CA | AU | TW | EU | FR |
|---|---|---|---|---|---|---|
| 150 mg/5 mL injection | Brineura 150mg/5ml solution for infusion vials | BRINEURA 150 mg, solution pour perfusion | ||||
| 150 mg per mL / per unit basis not stated cannot compare injection | BRINEURA 150 mg solution for infusion 倍原力150毫克輸注液 | |||||
| 30 mg/1 mL liquid | Brineura | |||||
| 30 mg/mL per mL / per unit basis not stated cannot compare injection | BRINEURA cerliponase alfa (rch) 150 mg/5 mL solution for injection vial with flushing solution vial | |||||
unknown | Brineura | Brineura |
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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 · FR and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en GB · FR que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 GB · FR 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 GB · FR 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.
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.