Depemokimab
ATC R03DX12 · 7 markets · 12 records
AU 3 records · 2 strengths
- 100 mginjectionEXDENSUR depemokimab 100 mg solution for injection in pre-filled penEXDENSUR depemokimab 100 mg solution for injection in pre-filled syringe
Records without a stated strength · 1 Exdensur
GB 2 records · 1 strengths
- 100 mg/1 mLinjectionExdensur 100mg/1ml solution for injection pre-filled pensExdensur 100mg/1ml solution for injection pre-filled syringes
CA 2 records · 1 strengths
- 100 mgliquidExdensur
US 1 records · 1 strengths
- 100 mginjectionExdensur
ES 1 records · 1 strengths
- 100 mginjectionEXDENSUR PRECARGADA
MX 1 records · 1 strengths
Records without a stated strength · 1 Exdensur
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 Exdensur
| Strength / form / release | US | GB | CA | AU | ES | MX | EU |
|---|---|---|---|---|---|---|---|
| 100 mg injection | Exdensur | EXDENSUR depemokimab 100 mg solution for injection in pre-filled pen EXDENSUR depemokimab 100 mg solution for injection in pre-filled syringe | EXDENSUR PRECARGADA | ||||
| 100 mg/1 mL injection | Exdensur 100mg/1ml solution for injection pre-filled pens Exdensur 100mg/1ml solution for injection pre-filled syringes | ||||||
| 100 mg liquid | Exdensur | ||||||
unknown | Exdensur | Exdensur | |||||
liquid | Exdensur |
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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 · MX and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en CA · MX que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 CA · MX 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 CA · MX 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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.