Datopotamab Deruxtecan
ATC L01FX35 · 8 markets · 8 records
US 1 records · 1 strengths
- 100 mg/5 mLinjectionDATROWAY
AU 1 records · 1 strengths
- 100 mginjectionDATROWAY datopotamab deruxtecan 100 mg powder for injection vial
SG 1 records · 1 strengths
- 100 mg/vialinjectionDATROWAY POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/VIAL
MX 1 records · 1 strengths
Records without a stated strength · 1 DATROWAY
TW 1 records · 1 strengths
- 100 mginjectionDATROWAY 100 mg powder for concentrate for solution for infusion達卓優凍晶注射劑100毫克
HK 1 records · 1 strengths
Records without a stated strength · 1 DATROWAY 100 mg powder for concentrate for solution for infusion
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 DATROWAY
| Strength / form / release | US | AU | SG | MX | TW | HK | EU |
|---|---|---|---|---|---|---|---|
| 100 mg injection | DATROWAY datopotamab deruxtecan 100 mg powder for injection vial | DATROWAY 100 mg powder for concentrate for solution for infusion 達卓優凍晶注射劑100毫克 | |||||
| 100 mg/5 mL injection | DATROWAY | ||||||
| 100 mg/vial injection | DATROWAY POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/VIAL | ||||||
unknown | DATROWAY 100 mg powder for concentrate for solution for infusion | DATROWAY | |||||
liquid | DATROWAY |
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Each country column shows the locally registered trade names — not translations.
3 more strength/form rows are recorded only in SG · MX · HK · EU and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en SG · MX · HK · EU que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 SG · MX · HK · EU 有记录(未在本表显示)。 另有 3 個規格/劑型僅在 SG · MX · HK · EU 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.