Leniolisib

ATC L03AX22 · 5 markets · 8 records

Leniolisib 5 markets · 8 records Forms

Filters

MarketUS 3 AU 2 GB 1 CA 1 EU 1

Strength

US 3 records · 3 shown of 3 Source openFDA NDC Directory · Data as of 2026-10-23

70 mgtabletJoenja also in GB·CA
50 mgtabletJoenja
40 mgtabletJoenja

AU 2 records · 1 shown of 1 Source TGA、TGA CMI repository (consumer medic · Data as of 2026-10-28、live · some records have no stated strength · includes records with unknown status (not proof of sale)

85.26 mgtabletJOENJA leniolisib (as phosphate) 70 mg film coated tablets bottle unknown

1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商

With a brand name Con nombre comercial 有商品名有商品名Joenja ×6

Full list in the data package Lista completa en el paquete de datos 完整清单见数据包完整清單見資料包

GB 1 records · 1 shown of 1 Source NHSBSA dm+d · Data as of 2026-10-19

70 mgtabletJoenja also in US·CA

CA 1 records · 1 shown of 1 Source Health Canada Drug Product Databas · Data as of 2026-10-23

70 mgtabletJoenja also in US·GB

EU 1 records · 0 shown of 0 Source European Commission · Data as of 2026-11-03 · some records have no stated strength

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.

1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商

With a brand name Con nombre comercial 有商品名有商品名Joenja ×3

Full list in the data package Lista completa en el paquete de datos 完整清单见数据包完整清單見資料包

Side-by-side table

Strength / form / release	US	GB	CA	AU	EU
70 mg tablet	Joenja	Joenja	Joenja	not recorded	not recorded
85.26 mg tablet	not recorded	not recorded	not recorded	JOENJA leniolisib (as phosphate) 70 mg film coated tablets bottle	not recorded
50 mg tablet	Joenja	not recorded	not recorded	not recorded	not recorded
40 mg tablet	Joenja	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	Joenja	Joenja

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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.

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.

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The same ingredient can carry completely different brand names in different countries, and the same name can point to a different ingredient. Listed by country — not interchangeable.

Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.