Daratumumab
ATC L01FC01 · 9 markets · 39 records
AU 10 records · 7 strengths
- 100 mg/5 mLinjectionDARZALEX
- 1,800 mg/15 mLinjectionDarzalex SC
- 1,800 mginjectionDARZALEX SC daratumumab 1800 mg/15 mL solution for injection vial
- 400 mg/20 mLinjectionDARZALEX
- 400 mginjectionDARZALEX daratumumab 100 mg/5 mL concentrated solution for infusion vial
- 100 mginjectionDARZALEX daratumumab 100 mg/5 mL concentrated solution for infusion vial
Records without a stated strength · 1 DARZALEX、Darzalex SC
ES 7 records · 2 strengths
US 3 records · 2 strengths
- 100 mg/5 mLinjectionDARZALEXDarzalex IV
- 1,800 mg/15 mLinjectionDarzalex Faspro
GB 3 records · 3 strengths
- 100 mg/5 mLinjectionDarzalex 100mg/5ml concentrate for solution for infusion vials
- 1,800 mg/15 mLinjectionDarzalex 1800mg/15ml solution for injection vials
- 400 mg/20 mLinjectionDarzalex 100mg/5ml concentrate for solution for infusion vials
CA 3 records · 2 strengths
- 120 mg/1 mLliquidDarzalex SC
- 20 mg/1 mLliquidDARZALEX
SG 3 records · 3 strengths
- 100 mg/5 mLinjectionDARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 400MG/20ML
- 1,800 mg/15 mLinjectionDARZALEX SC SOLUTION FOR INJECTION 1800MG/15ML
- 400 mg/20 mLinjectionDARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 400MG/20ML
HK 3 records · 1 strengths
Records without a stated strength · 1 Darzalex 1800mg solution for subcutaneous injection、DARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/5ML (SWITZERLAND)、DARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 400MG/20ML
TW 2 records · 2 strengths
- 1,800 mginjectionDarzalex 1800mg solution for subcutaneous兆科皮下注射劑1800毫克
Records without a stated strength · 1 Darzalex Concentrate for solution for infusion 20mg/ml、兆科注射劑20毫克/毫升
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 DARZALEX
| Strength / form / release | US | GB | CA | AU | SG | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 100 mg/5 mL injection | DARZALEX Darzalex IV | Darzalex 100mg/5ml concentrate for solution for infusion vials | DARZALEX | DARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 400MG/20ML | |||||
| 1,800 mg/15 mLRecorded as: 1.8 g/15 mL injection | Darzalex Faspro | Darzalex 1800mg/15ml solution for injection vials | Darzalex SC | DARZALEX SC SOLUTION FOR INJECTION 1800MG/15ML | |||||
| 1,800 mg injection | DARZALEX SC daratumumab 1800 mg/15 mL solution for injection vial | DARZALEX | Darzalex 1800mg solution for subcutaneous 兆科皮下注射劑1800毫克 | ||||||
| 400 mg/20 mL injection | Darzalex 100mg/5ml concentrate for solution for infusion vials | DARZALEX | DARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 400MG/20ML | ||||||
| 120 mg/1 mL liquid | Darzalex SC | ||||||||
| 20 mg/1 mL liquid | DARZALEX | ||||||||
| 400 mg injection | DARZALEX daratumumab 100 mg/5 mL concentrated solution for infusion vial | ||||||||
| 100 mg injection | DARZALEX daratumumab 100 mg/5 mL concentrated solution for infusion vial | ||||||||
| 20 mg/1 mL injection | DARZALEX | ||||||||
unknown | DARZALEX Darzalex SC | Darzalex 1800mg solution for subcutaneous injection DARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/5ML (SWITZERLAND) DARZALEX CONCENTRATE FOR SOLUTION FOR INFUSION 400MG/20ML | DARZALEX | ||||||
injection | Darzalex Concentrate for solution for infusion 20mg/ml 兆科注射劑20毫克/毫升 |
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Each country column shows the locally registered trade names — not translations.
3 more strength/form rows are recorded only in CA · ES and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en CA · ES que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 CA · ES 有记录(未在本表显示)。 另有 3 個規格/劑型僅在 CA · ES 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.