Trametinib
ATC L01EE01 · 8 markets · 26 records
GB 6 records · 3 strengths
- 2 mgtabletMekinist
Records without a stated strength · 2 Mekinist Spexotras 50micrograms/ml oral solution
CN 4 records · 2 strengths
ES 4 records · 3 strengths
CA 3 records · 3 strengths
AU 3 records · 3 strengths
HK 2 records · 1 strengths
Records without a stated strength · 1 Mekinist
EU 2 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 Mekinist、SPEXOTRAS
SG 1 records · 1 strengths
- 4.7 mgpowderMEKINIST® POWDER FOR ORAL SOLUTION 4.7 MG
| Strength / form / release | GB | CA | AU | SG | CN | ES | HK | EU |
|---|---|---|---|---|---|---|---|---|
| 2 mg tablet | Mekinist | Mekinist | Mekinist | 迈吉宁曲美替尼 | Mekinist | |||
| 0.5 mgRecorded as: 500 microgram tablet | Mekinist | Mekinist | 迈吉宁曲美替尼 | Mekinist | ||||
| 4.7 mg powder | Mekinist | MEKINIST® POWDER FOR ORAL SOLUTION 4.7 MG | ||||||
| 4.7 mg liquid | SPEXOTRAS | |||||||
| 0.05 mg/1 mLRecorded as: 50 microgram/1 mL powder | Mekinist | |||||||
unknown | Mekinist | Mekinist SPEXOTRAS | ||||||
tablet | Mekinist | |||||||
liquid | Spexotras 50micrograms/ml oral solution |
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Each country column shows the locally registered trade names — not translations.
3 more strength/form rows are recorded only in GB · HK · EU and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en GB · HK · EU que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 GB · HK · EU 有记录(未在本表显示)。 另有 3 個規格/劑型僅在 GB · 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.