Lurbinectedin
ATC L01XX69 · 8 markets · 11 records
AU 3 records · 3 strengths
- 4 mginjectionZEPZELCA lurbinectedin 4 mg powder for solution for infusion 1 vial per carton
- 2 mginjectionZEPZELCA lurbinectedin 2 mg powder for solution for infusion vial
Records without a stated strength · 1 ZEPZELCA
US 1 records · 1 strengths
- 0.5 mginjectionZEPZELCA
SG 1 records · 1 strengths
- 4 mg/vialinjectionZEPZELCA POWDER FOR SOLUTION FOR INFUSION 4MG/VIAL
TW 1 records · 1 strengths
- 4 mginjectionZEPZELCA lyophilized powder for solution for infusion 4 mg贊必佳凍晶注射劑4毫克
HK 1 records · 1 strengths
Records without a stated strength · 1 ZEPZELCA POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 4MG
EU 1 records · 1 strengths
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.
Records without a stated strength · 1 ZEPZELCA
| Strength / form / release | US | AU | SG | TW | HK | EU |
|---|---|---|---|---|---|---|
| 4 mg injection | ZEPZELCA lurbinectedin 4 mg powder for solution for infusion 1 vial per carton | ZEPZELCA lyophilized powder for solution for infusion 4 mg 贊必佳凍晶注射劑4毫克 | ||||
| 4 mg/vial injection | ZEPZELCA POWDER FOR SOLUTION FOR INFUSION 4MG/VIAL | |||||
| 2 mg injection | ZEPZELCA lurbinectedin 2 mg powder for solution for infusion vial | |||||
| 0.5 mg injection | ZEPZELCA | |||||
unknown | ZEPZELCA | ZEPZELCA POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 4MG | ZEPZELCA |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in SG and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en SG que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 SG 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 SG 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.