Avatrombopag
Records for this ingredient, by country (identity only).
ATC B02BX08 · 8 markets · 11 records
AU 3 records · 2 shown of 2
- 20 mgtabletDOPTELET
- 23.6 mgtabletDOPTELET avatrombopag (as maleate) 20 mg film-coated tablets blister pack
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
US 2 records · 2 shown of 2
- 20 mgtabletDOPTELET
- 10 mgpowderDoptelet Sprinkle
GB 1 records · 1 shown of 1
- 20 mgtabletDOPTELET
CA 1 records · 1 shown of 1
- 20 mgtabletDOPTELET
ES 1 records · 1 shown of 1
- 20 mgtabletDOPTELET
HK 1 records · 0 shown of 0
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
JP 1 records · 1 shown of 1
- 20 mgtabletドプテレット錠20mg
EU 1 records · 0 shown of 0
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 | AU | ES | HK | JP | EU |
|---|---|---|---|---|---|---|---|---|
| 20 mg tablet | DOPTELET | DOPTELET | DOPTELET | DOPTELET | DOPTELET | ドプテレット錠20mg | ||
| 23.6 mg tablet | DOPTELET avatrombopag (as maleate) 20 mg film-coated tablets blister pack | |||||||
| 10 mg powder | Doptelet Sprinkle | |||||||
unknown | DOPTELET | DOPTELET | DOPTELET |
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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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.