Pegvisomant
ATC H01AX01 · 6 markets · 29 records
AU 7 records · 4 strengths
- 20 mginjectionSOMAVERTSOMAVERT pegvisomant (rbe) 10mg powder for injection vial and diluent in pre-filled syringe
- 15 mginjectionSOMAVERTSOMAVERT pegvisomant (rbe) 10mg powder for injection vial and diluent in pre-filled syringe
- 10 mginjectionSOMAVERTSOMAVERT pegvisomant (rbe) 10mg powder for injection vial and diluent in pre-filled syringe
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
GB 5 records · 5 strengths
- 20 mginjectionSomavert 10mg powder and solvent for solution for injection vials
- 15 mginjectionSomavert 10mg powder and solvent for solution for injection vials
- 10 mginjectionSomavert 10mg powder and solvent for solution for injection vials
- 30 mginjectionSomavert 10mg powder and solvent for solution for injection vials
- 25 mginjectionSomavert 10mg powder and solvent for solution for injection vials
CA 5 records · 5 strengths
ES 5 records · 5 strengths
FR 5 records · 5 strengths
- 20 mginjectionSOMAVERT 10 mg, poudre et solvant pour solution injectable
- 15 mginjectionSOMAVERT 10 mg, poudre et solvant pour solution injectable
- 10 mginjectionSOMAVERT 10 mg, poudre et solvant pour solution injectable
- 30 mginjectionSOMAVERT 10 mg, poudre et solvant pour solution injectable
- 25 mginjectionSOMAVERT 10 mg, poudre et solvant pour solution injectable
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.
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
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Each country column shows the locally registered trade names — not translations.
“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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.