Encorafenib
ATC L01EC03 · 10 markets · 19 records
AU 5 records · 3 strengths
- 75 mgcapsuleBRAFTOVIBRAFTOVI encorafenib 75 mg capsule blister pack
- 50 mgcapsuleBRAFTOVIBRAFTOVI encorafenib 75 mg capsule blister pack
Records without a stated strength · 1 BRAFTOVI
GB 3 records · 2 strengths
SG 2 records · 2 strengths
- 75 mgcapsuleBraftovi 75 mg hard capsules
- 50 mgcapsuleBraftovi 75 mg hard capsules
ES 2 records · 2 strengths
HK 2 records · 1 strengths
Records without a stated strength · 1 BRAFTOVI
US 1 records · 1 strengths
- 75 mgcapsuleBRAFTOVI
CA 1 records · 1 strengths
- 75 mgcapsuleBRAFTOVI
MX 1 records · 1 strengths
Records without a stated strength · 1 BRAFTOVI
TW 1 records · 1 strengths
- 75 mgcapsuleBraftovi 75 mg hard capsules迫癌癒 75 毫克膠囊
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.
Records without a stated strength · 1 BRAFTOVI
| Strength / form / release | US | GB | CA | AU | SG | ES | MX | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 75 mg capsule | BRAFTOVI | BRAFTOVI | BRAFTOVI | BRAFTOVI BRAFTOVI encorafenib 75 mg capsule blister pack | Braftovi 75 mg hard capsules | BRAFTOVI | Braftovi 75 mg hard capsules 迫癌癒 75 毫克膠囊 | |||
| 50 mg capsule | BRAFTOVI | BRAFTOVI BRAFTOVI encorafenib 75 mg capsule blister pack | Braftovi 75 mg hard capsules | BRAFTOVI | ||||||
unknown | BRAFTOVI | BRAFTOVI | BRAFTOVI | |||||||
capsule | BRAFTOVI |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in MX and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en MX que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 MX 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 MX 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.