Gemtuzumab Ozogamicin
ATC L01FX02 · 9 markets · 12 records
AU 3 records · 2 strengths
- 5 mginjectionMylotargMYLOTARG gemtuzumab ozogamicin 5 mg powder for injection vial
Records without a stated strength · 1 Mylotarg
EU 2 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 Mylotarg、Mylotarg Refusal
US 1 records · 1 strengths
- 5 mg/5 mLinjectionMylotarg
GB 1 records · 1 strengths
- 5 mginjectionMylotarg 5mg powder for concentrate for solution for infusion vials
CA 1 records · 1 strengths
- 4.5 mgpowderMylotarg
SG 1 records · 1 strengths
- 5 mg/vialpowderMYLOTARG POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 5MG/VIAL
ES 1 records · 1 strengths
- 5 mginjectionMylotarg
TW 1 records · 1 strengths
- 5 mginjectionMYLOTARG 5 mg powder for concentrate for solution for infusion滅髓瘤凍晶注射劑5毫克
HK 1 records · 1 strengths
Records without a stated strength · 1 MYLOTARG 5 mg powder for concentrate for solution for infusion
| Strength / form / release | US | GB | CA | AU | SG | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 5 mg injection | Mylotarg 5mg powder for concentrate for solution for infusion vials | Mylotarg MYLOTARG gemtuzumab ozogamicin 5 mg powder for injection vial | Mylotarg | MYLOTARG 5 mg powder for concentrate for solution for infusion 滅髓瘤凍晶注射劑5毫克 | |||||
| 5 mg/5 mL injection | Mylotarg | ||||||||
| 5 mg/vial powder | MYLOTARG POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 5MG/VIAL | ||||||||
| 4.5 mg powder | Mylotarg | ||||||||
unknown | Mylotarg | MYLOTARG 5 mg powder for concentrate for solution for infusion | Mylotarg Mylotarg Refusal |
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Each country column shows the locally registered trade names — not translations.
2 more strength/form rows are recorded only in CA · SG and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en CA · SG que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 CA · SG 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 CA · 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.