Tebentafusp

ATC L01XX75 · 6 markets · 8 records

Tebentafusp 6 markets · 8 records Forms

AU 3 records · 3 strengths

0.1 mg/0.5 mLinjectionKIMMTRAK also in US·ES
0.2 mg/mLinjectionKIMMTRAK tebentafusp 0.1 mg/0.5 mL concentrated solution for infusion vial unknown

Records without a stated strength · 1 KIMMTRAK

US 1 records · 1 strengths

0.1 mg/0.5 mLinjectionKIMMTRAK also in AU·ES

GB 1 records · 1 strengths

0.5 mLinjectionKimmtrak 100micrograms/0.5ml concentrate for solution for infusion vials

CA 1 records · 1 strengths

0.1 mgliquidKIMMTRAK

ES 1 records · 1 strengths

0.1 mg/0.5 mLinjectionKIMMTRAK also in AU·US

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 KIMMTRAK

Side-by-side table

Strength / form / release	US	GB	CA	AU	ES	EU
0.1 mg/0.5 mLRecorded as: 100 mcg/0.5 mL、100 microgram/0.5 mL、100 ug/0.5 mL injection	KIMMTRAK	not recorded	not recorded	KIMMTRAK	KIMMTRAK	not recorded
0.1 mgRecorded as: 100 mcg liquid	not recorded	not recorded	KIMMTRAK	not recorded	not recorded	not recorded
0.5 mL injection	not recorded	Kimmtrak 100micrograms/0.5ml concentrate for solution for infusion vials	not recorded	not recorded	not recorded	not recorded
0.2 mg/mL injection	not recorded	not recorded	not recorded	KIMMTRAK tebentafusp 0.1 mg/0.5 mL concentrated solution for infusion vial	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	KIMMTRAK	not recorded	KIMMTRAK

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

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

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.