Capmatinib
Records for this ingredient, by country (identity only).
ATC L01EP01 · 9 markets · 19 records
US 4 records · 2 shown of 2
AU 2 records · 2 shown of 2
- 244 mgtabletTABRECTA capmatinib (as hydrochloride) 150 mg tablet blister pack
- 183 mgtabletTABRECTA capmatinib (as hydrochloride) 150 mg tablet blister pack
HK 2 records · 0 shown of 0
2 records · 0 manufacturers 2 registros · 0 fabricantes 2 个记录 · 0 个厂家 2 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 2 records · 2 shown of 2
- 200 mgtabletタブレクタ錠200mg
- 150 mgtabletタブレクタ錠200mg
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 | CA | AU | SG | ES | TW | HK | JP | EU |
|---|---|---|---|---|---|---|---|---|---|
| 200 mg tablet | Manufacturer: Novartis Pharma Produktions… ×2 TABRECTA | TABRECTA | TABRECTA | TABRECTA | TABRECTA 泰芮塔200毫克膜衣錠 | タブレクタ錠200mg | |||
| 150 mg tablet | Manufacturer: Novartis Pharma Produktions… ×2 TABRECTA | TABRECTA | TABRECTA | TABRECTA | TABRECTA 泰芮塔150毫克膜衣錠 | タブレクタ錠200mg | |||
| 244 mg tablet | TABRECTA capmatinib (as hydrochloride) 150 mg tablet blister pack | ||||||||
| 183 mg tablet | TABRECTA capmatinib (as hydrochloride) 150 mg tablet blister pack | ||||||||
unknown | TABRECTA | TABRECTA |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in HK · EU and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en HK · EU que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 HK · EU 有记录（未在本表显示）。 另有 1 個規格/劑型僅在 HK · EU 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.