Crizotinib
ATC L01ED01 · 10 markets · 33 records
US 5 records · 5 strengths
GB 5 records · 2 strengths
AU 5 records · 3 strengths
- 250 mgcapsuleXalkoriXALKORI crizotinib 200 mg capsule blister pack
- 200 mgcapsuleXalkoriXALKORI crizotinib 200 mg capsule blister pack
Records without a stated strength · 1 Xalkori
ES 5 records · 5 strengths
- 250 mgcapsuleXalkori
- 200 mgcapsuleXalkori
- 150 mgcapsuleXALKORI ABRIR
- 50 mgcapsuleXALKORI ABRIR
- 20 mgcapsuleXALKORI ABRIR
CN 4 records · 2 strengths
CA 2 records · 2 strengths
SG 2 records · 2 strengths
TW 2 records · 2 strengths
HK 2 records · 1 strengths
Records without a stated strength · 1 Xalkori
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 Xalkori
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 250 mgRecorded as: 0.25 g capsule | Xalkori | Xalkori | Xalkori | Xalkori XALKORI crizotinib 200 mg capsule blister pack | Xalkori | 赛可瑞克唑替尼 | Xalkori | Xalkori 截剋瘤膠囊250毫克 | ||
| 200 mgRecorded as: 0.2 g capsule | Xalkori | Xalkori | Xalkori | Xalkori XALKORI crizotinib 200 mg capsule blister pack | Xalkori | 赛可瑞克唑替尼 | Xalkori | Xalkori 截剋瘤膠囊200毫克 | ||
| 150 mg capsule | Xalkori | XALKORI ABRIR | ||||||||
| 50 mg capsule | Xalkori | XALKORI ABRIR | ||||||||
| 20 mg capsule | Xalkori | XALKORI ABRIR | ||||||||
unknown | Xalkori | Xalkori | Xalkori |
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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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.