Tralokinumab
ATC D11AH07 · 6 markets · 11 records
US 2 records · 2 strengths
GB 2 records · 2 strengths
- 300 mg/2 mLinjectionAdtralza 300mg/2ml solution for injection pre-filled pens
- 150 mg/1 mLinjectionAdtralza 150mg/1ml solution for injection pre-filled syringes
CA 2 records · 2 strengths
ES 2 records · 2 strengths
- 150 mginjectionADTRALZA PRECARGADA
- 300 mginjectionADTRALZA PRECARGADA
FR 2 records · 2 strengths
- 300 mg/2 mLinjectionADTRALZA 300 mg, solution injectable en stylo prérempli
- 150 mg/1 mLinjectionADTRALZA 150 mg, solution injectable en seringue préremplie
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
| Strength / form / release | US | GB | CA | ES | EU | FR |
|---|---|---|---|---|---|---|
| 300 mg/2 mL injection | Adbry | Adtralza 300mg/2ml solution for injection pre-filled pens | ADTRALZA 300 mg, solution injectable en stylo prérempli | |||
| 150 mg injection | Adbry | ADTRALZA PRECARGADA | ||||
| 150 mg/1 mL injection | Adtralza 150mg/1ml solution for injection pre-filled syringes | ADTRALZA 150 mg, solution injectable en seringue préremplie | ||||
| 150 mg liquid | ADTRALZA | |||||
| 150 mg/1 mL liquid | ADTRALZA | |||||
| 300 mg injection | ADTRALZA PRECARGADA | |||||
unknown | ADTRALZA |
Scroll horizontally for more markets →
Each country column shows the locally registered trade names — not translations.
2 more strength/form rows are recorded only in GB · EU · FR and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en GB · EU · FR que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 GB · EU · FR 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 GB · EU · FR 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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.