Mecasermin
ATC H01AC03 · 7 markets · 11 records
US 3 records · 2 strengths
- 40 mg/4 mLinjectionIncrelex
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
AU 3 records · 3 strengths
- 10 mg/1 mLinjectionIncrelex
- 10 mg/mLinjectionINCRELEX mecasermin 10 mg/mL solution for injection vial
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 1 records · 1 strengths
- 40 mg/4 mLinjectionIncrelex 40mg/4ml solution for injection vials
CA 1 records · 1 strengths
- 10 mgliquidIncrelex
ES 1 records · 1 strengths
- 10 mginjectionIncrelex
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
FR 1 records · 1 strengths
- 10 mg/1 mLinjectionINCRELEX 10 mg/ml, solution injectable
| Strength / form / release | US | GB | CA | AU | ES | EU | FR |
|---|---|---|---|---|---|---|---|
| 40 mg/4 mL injection | Increlex | Increlex 40mg/4ml solution for injection vials | |||||
| 10 mg/1 mL injection | Increlex | INCRELEX 10 mg/ml, solution injectable | |||||
| 10 mg liquid | Increlex | ||||||
| 10 mg injection | Increlex | ||||||
| 10 mg/mL injection | INCRELEX mecasermin 10 mg/mL solution for injection vial | ||||||
unknown | Increlex | Increlex | |||||
liquid | GUNA-IGF |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in ES and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en ES que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 ES 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 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.
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.