Ravulizumab

ATC L04AJ02 · 9 markets · 22 records

Ravulizumab 9 markets · 22 records Forms

AU 5 records · 4 strengths

1,100 mg/11 mLinjectionUltomiris also in GB·ES
300 mg/3 mLinjectionUltomiris also in GB·ES
100 mg/mLinjectionULTOMIRIS ravulizumab rch 300 mg in 3 mL (100 mg/mL) concentrated solution for injection by intravenous infusion vial also in SG unknown

Records without a stated strength · 1 Ultomiris 100mg/ml

US 3 records · 3 strengths

1,100 mg/11 mLliquidUltomiris
300 mg/3 mLliquidUltomiris
300 mg/30 mLliquidUltomiris

GB 3 records · 3 strengths

1,100 mg/11 mLinjectionUltomiris 300mg/30ml concentrate for solution for infusion vials also in AU·ES
300 mg/3 mLinjectionUltomiris 300mg/30ml concentrate for solution for infusion vials also in AU·ES
300 mg/30 mLinjectionUltomiris 300mg/30ml concentrate for solution for infusion vials

CA 2 records · 1 strengths

100 mg/1 mLliquidUltomiris

ES 2 records · 2 strengths

1,100 mg/11 mLinjectionUltomiris also in AU·GB
300 mg/3 mLinjectionUltomiris also in AU·GB

TW 2 records · 1 strengths

100 mginjectionUltomiris concentrate for solution for infusion 100mg/ml+2優力適輸注液100毫克/毫升、妥立瑞輸注液100毫克/毫升

HK 2 records · 1 strengths

Records without a stated strength · 1 ULTOMIRIS CONCENTRATE FOR SOLUTION FOR INFUSION 1100MG/11ML

SG 1 records · 1 strengths

100 mg/mLinjectionUltomiris concentrate for solution for infusion 100mg/ml also in AU

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 Ultomiris

Side-by-side table

Strength / form / release	US	GB	CA	AU	SG	ES	TW	HK	EU
1,100 mg/11 mLRecorded as: 1.1 g/11 mL injection	not recorded	Ultomiris 300mg/30ml concentrate for solution for infusion vials	not recorded	Ultomiris	not recorded	Ultomiris	not recorded	not recorded	not recorded
300 mg/3 mL injection	not recorded	Ultomiris 300mg/30ml concentrate for solution for infusion vials	not recorded	Ultomiris	not recorded	Ultomiris	not recorded	not recorded	not recorded
100 mg injection	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	Ultomiris concentrate for solution for infusion 100mg/ml 優力適輸注液100毫克/毫升妥立瑞輸注液100毫克/毫升	not recorded	not recorded
100 mg/mL injection	not recorded	not recorded	not recorded	ULTOMIRIS ravulizumab rch 300 mg in 3 mL (100 mg/mL) concentrated solution for injection by intravenous infusion vial	Ultomiris concentrate for solution for infusion 100mg/ml	not recorded	not recorded	not recorded	not recorded
1,100 mg/11 mL liquid	Ultomiris	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
300 mg/3 mL liquid	Ultomiris	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
300 mg/30 mL liquid	Ultomiris	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
100 mg/1 mL liquid	not recorded	not recorded	Ultomiris	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
300 mg/30 mL injection	not recorded	Ultomiris 300mg/30ml concentrate for solution for infusion vials	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	Ultomiris 100mg/ml	not recorded	not recorded	not recorded	ULTOMIRIS CONCENTRATE FOR SOLUTION FOR INFUSION 1100MG/11ML	Ultomiris

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

2 more strength/form rows are recorded only in CA · TW and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en CA · TW que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 CA · TW 有记录（未在本表显示）。另有 2 個規格/劑型僅在 CA · TW 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.