Clesrovimab
ATC J06BD10 · 8 markets · 9 records
AU 2 records · 2 strengths
- 105 mginjectionENFLONSIA clesrovimab 105 mg in 0.7 mL solution for injection prefilled syringe
Records without a stated strength · 1 ENFLONSIA
US 1 records · 1 strengths
- 150 mginjectionENFLONSIA
GB 1 records · 1 strengths
- 105 mg/0.7 mLinjectionEnflonsia 105mg/0.7ml solution for injection pre-filled syringes
CA 1 records · 1 strengths
- 105 mgliquidENFLONSIA
SG 1 records · 1 strengths
- 105 mg/0.7 mLinjectionENFLONSIA™ SOLUTION FOR INJECTION 105MG/0.7ML IN PRE-FILLED SYRINGE
ES 1 records · 1 strengths
- 105 mginjectionENFLONSIA PRECARGADA
MX 1 records · 1 strengths
Records without a stated strength · 1 ENFLONSIA
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 ENFLONSIA
| Strength / form / release | US | GB | CA | AU | SG | ES | MX | EU |
|---|---|---|---|---|---|---|---|---|
| 105 mg/0.7 mL injection | Enflonsia 105mg/0.7ml solution for injection pre-filled syringes | ENFLONSIA™ SOLUTION FOR INJECTION 105MG/0.7ML IN PRE-FILLED SYRINGE | ||||||
| 105 mg injection | ENFLONSIA clesrovimab 105 mg in 0.7 mL solution for injection prefilled syringe | ENFLONSIA PRECARGADA | ||||||
| 105 mg liquid | ENFLONSIA | |||||||
| 150 mg injection | ENFLONSIA | |||||||
unknown | ENFLONSIA | ENFLONSIA | ||||||
liquid | ENFLONSIA |
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Each country column shows the locally registered trade names — not translations.
2 more strength/form rows are recorded only in GB · SG · MX and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en GB · SG · MX que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 GB · SG · MX 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 GB · SG · 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.