Elotuzumab
ATC L01FX08 · 8 markets · 16 records
AU 5 records · 5 strengths
- 400 mginjectionEMPLICITI
- 300 mginjectionEMPLICITI
- 440 mginjectionEMPLICITI elotuzumab 300mg lyophilized powder for IV infusion vial
- 340 mginjectionEMPLICITI elotuzumab 300mg lyophilized powder for IV infusion vial
Records without a stated strength · 1 EMPLICITI
US 2 records · 2 strengths
GB 2 records · 2 strengths
HK 2 records · 1 strengths
Records without a stated strength · 1 EMPLICITI POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 300MG
ES 1 records · 1 strengths
- 400 mginjectionEMPLICITI
TW 1 records · 1 strengths
Records without a stated strength · 1 Empliciti TM (elotuzumab) For Injection、恩必喜凍晶注射劑
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 EMPLICITI
| Strength / form / release | US | GB | AU | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|
| 400 mg injection | EMPLICITI | Empliciti 400mg powder for concentrate for solution for infusion vials | EMPLICITI | EMPLICITI | |||
| 300 mg injection | EMPLICITI | Empliciti 400mg powder for concentrate for solution for infusion vials | EMPLICITI | ||||
| 440 mg injection | EMPLICITI elotuzumab 300mg lyophilized powder for IV infusion vial | ||||||
| 340 mg injection | EMPLICITI elotuzumab 300mg lyophilized powder for IV infusion vial | ||||||
unknown | EMPLICITI | EMPLICITI POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 300MG | EMPLICITI | ||||
injection | Empliciti TM (elotuzumab) For 恩必喜凍晶注射劑 |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in TW and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en TW que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 TW 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 TW 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.