Niraparib
ATC L01XK02 · 10 markets · 33 records
US 5 records · 4 strengths
GB 5 records · 3 strengths
HK 4 records · 1 strengths
Records without a stated strength · 1 AKEEGA、ZEJULA
CA 3 records · 2 strengths
ES 3 records · 2 strengths
TW 3 records · 2 strengths
- 100 mgtabletZEJULA截永樂錠100毫克
Records without a stated strength · 1 AKEEGA、澤截膜衣錠100/500毫克、澤截膜衣錠50/500毫克
AU 2 records · 1 strengths
- 100 mgtabletZEJULA
SG 2 records · 2 strengths
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 AKEEGA、ZEJULA
MX 1 records · 1 strengths
Records without a stated strength · 1 AKEEGA
| Strength / form / release | US | GB | CA | AU | SG | ES | MX | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 100 mg tablet | AKEEGA ZEJULA | AKEEGA ZEJULA | AKEEGA ZEJULA | ZEJULA | ZEJULA | AKEEGA ZEJULA | ZEJULA 截永樂錠100毫克 | |||
| 50 mg tablet | AKEEGA | AKEEGA | AKEEGA | AKEEGA | ||||||
| 200 mg tablet | ZEJULA | ZEJULA | ||||||||
| 300 mg tablet | ZEJULA | |||||||||
| 100 mg capsule | ZEJULA | |||||||||
tablet | AKEEGA | AKEEGA 澤截膜衣錠100/500毫克 澤截膜衣錠50/500毫克 | ||||||||
unknown | AKEEGA ZEJULA | AKEEGA ZEJULA |
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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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.