Pertuzumab
ATC L01FD02 · 11 markets · 48 records
ES 9 records · 3 strengths
AU 5 records · 5 strengths
- 420 mginjectionPERJETA pertuzumab (rch) 30mg/mL concentrate injection vial
- 1,200 mginjectionPHESGO SC pertuzumab (rch) 1200mg and trastuzumab (rch) 600mg in 15mL solution for injection, vials
- 600 mginjectionPHESGO SC pertuzumab (rch) 1200mg and trastuzumab (rch) 600mg in 15mL solution for injection, vials
- 420 mg/14 mLinjectionPERJETA
Records without a stated strength · 1 PERJETA
GB 4 records · 3 strengths
- 1,200 mg/15 mLinjectionPhesgo 600mg/600mg/10ml solution for injection vials
- 600 mg/10 mLinjectionPhesgo 600mg/600mg/10ml solution for injection vials
- 420 mg/14 mLinjectionPerjeta 420mg/14ml concentrate for solution for infusion vials
CA 4 records · 3 strengths
CN 4 records · 1 strengths
- 420 mginjection安赛珠帕妥珠单抗帕乐坦、帕捷特
US 3 records · 3 strengths
SG 3 records · 3 strengths
- 1,200 mginjectionPhesgo Solution for Subcutaneous Injection 1200/600 mg
- 600 mginjectionPhesgo Solution for Subcutaneous Injection 1200/600 mg
- 30 mg/mLinjectionPERJETA CONCENTRATE FOR SOLUTION FOR INFUSION 420MG/14ML
TW 3 records · 2 strengths
- 420 mginjectionPerjeta Vial 420mg賀疾妥注射液420毫克
Records without a stated strength · 1 Phesgo Solution for Subcutaneous Injection 1200/600 mg、賀雙妥皮下注射劑 1200/600毫克、賀雙妥皮下注射劑 600/600毫克
HK 3 records · 1 strengths
Records without a stated strength · 1 PERJETA CONCENTRATE FOR SOLUTION FOR INFUSION 420MG/14ML、PHESGO SOLUTION FOR SUBCUTANEOUS INJECTION 1200MG/600MG IN 15ML
EU 3 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 PERJETA、Phesgo、POHERDY
MX 1 records · 1 strengths
Records without a stated strength · 1 Phesgo
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Each country column shows the locally registered trade names — not translations.
5 more strength/form rows are recorded only in CA · SG · MX and are not shown in this table. Hay 5 filas de concentración/forma registradas solo en CA · SG · MX que no se muestran en esta tabla. 另有 5 个规格/剂型仅在 CA · SG · MX 有记录(未在本表显示)。 另有 5 個規格/劑型僅在 CA · 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.
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.