Ponatinib
ATC L01EA05 · 9 markets · 28 records
AU 7 records · 7 strengths
- 15 mgtabletIclusig
- 45 mgtabletIclusig
- 48.1 mgtabletICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle
- 32.05 mgtabletICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle
- 16 mgtabletICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle
- 10.68 mgtabletICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle
Records without a stated strength · 1 Iclusig
GB 6 records · 3 strengths
US 4 records · 4 strengths
ES 3 records · 3 strengths
SG 2 records · 2 strengths
HK 2 records · 1 strengths
Records without a stated strength · 1 Iclusig
CA 1 records · 1 strengths
- 15 mgtabletIclusig
CN 1 records · 1 strengths
- 15 mgtablet英可欣泊那替尼
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 Iclusig
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 15 mg tablet | Iclusig | No trade name Iclusig | Iclusig | Iclusig | Iclusig | 英可欣泊那替尼 | Iclusig | ||
| 45 mg tablet | Iclusig | No trade name Iclusig | Iclusig | Iclusig | Iclusig | ||||
| 30 mg tablet | Iclusig | No trade name Iclusig | Iclusig | ||||||
| 48.1 mg tablet | ICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle | ||||||||
| 32.05 mg tablet | ICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle | ||||||||
| 16 mg tablet | ICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle | ||||||||
| 10.68 mg tablet | ICLUSIG ponatinib (as hydrochloride) 15 mg film-coated tablet bottle | ||||||||
| 10 mg tablet | Iclusig | ||||||||
unknown | Iclusig | Iclusig | Iclusig |
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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.