Lurbinectedin

Records for this ingredient, by country (identity only).

ATC L01XX69 · 8 markets · 11 records

Lurbinectedin 8 markets · 11 records Forms

Filters

MarketAU 3 US 1 SG 1 TW 1 HK 1 EU 1

Strength

AU 3 records · 2 shown of 2 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)

4 mg per mL / per unit basis not statedinjectionZEPZELCA lurbinectedin 4 mg powder for solution for infusion 1 vial per carton unknown
2 mg per mL / per unit basis not statedinjectionZEPZELCA lurbinectedin 2 mg powder for solution for infusion vial 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ZEPZELCA ×1

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

US 1 records · 1 shown of 1 Source openFDA NDC Directory · Data as of 2026-10-23

0.5 mg per mL / per unit basis not statedinjectionZEPZELCA

SG 1 records · 1 shown of 1 Source Health Sciences Authority (HSA) · Data as of 2026-08-07

4 mg/vial per mL / per unit basis not statedinjectionZEPZELCA POWDER FOR SOLUTION FOR INFUSION 4MG/VIAL

TW 1 records · 1 shown of 1 Source 衛生福利部食品藥物管理署（TFDA）全部藥品許可證資料集 · Data as of 2026-10-22

4 mg per mL / per unit basis not statedinjectionZEPZELCA lyophilized powder for solution for infusion 4 mg+1贊必佳凍晶注射劑4毫克

HK 1 records · 0 shown of 0 Source 衞生署藥物辦公室（香港）註冊藥劑製品名單 · Data as of 2026-10-23 · some records have no stated strength · includes records with unknown status (not proof of sale)

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ZEPZELCA POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 4MG ×1

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

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ZEPZELCA ×1

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

Some strengths are recorded without a per mL / per unit basis. They are shown as recorded and are not compared with other markets.

Side-by-side table

Strength / form / release	US	AU	SG	TW	HK	EU
4 mg per mL / per unit basis not stated cannot compare injection	not recorded	ZEPZELCA lurbinectedin 4 mg powder for solution for infusion 1 vial per carton	not recorded	ZEPZELCA lyophilized powder for solution for infusion 4 mg 贊必佳凍晶注射劑4毫克	not recorded	not recorded
4 mg/vial per mL / per unit basis not stated cannot compare injection	not recorded	not recorded	ZEPZELCA POWDER FOR SOLUTION FOR INFUSION 4MG/VIAL	not recorded	not recorded	not recorded
2 mg per mL / per unit basis not stated cannot compare injection	not recorded	ZEPZELCA lurbinectedin 2 mg powder for solution for infusion vial	not recorded	not recorded	not recorded	not recorded
0.5 mg per mL / per unit basis not stated cannot compare injection	ZEPZELCA	not recorded	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	ZEPZELCA	not recorded	not recorded	ZEPZELCA POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION 4MG	ZEPZELCA

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Each country column shows the locally registered trade names — not translations.

1 more strength/form rows are recorded only in SG and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en SG que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 SG 有记录（未在本表显示）。另有 1 個規格/劑型僅在 SG 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.

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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.