Elosulfase Alfa

ATC A16AB12 · 6 markets · 8 records

Elosulfase Alfa 6 markets · 8 records Forms

GB 2 records · 1 strengths

5 mg/5 mLinjectionVimizim 5mg/5ml concentrate for solution for infusion vials+1Vimizim 5mg/5ml solution for infusion vials also in US

AU 2 records · 2 strengths

1 mg/mLinjectionVIMIZIM elosulfase alfa (rch) 1 mg/mL concentrated solution for injection vial unknown

Records without a stated strength · 1 VIMIZIM

US 1 records · 1 strengths

5 mg/5 mLinjectionVIMIZIM also in GB

CA 1 records · 1 strengths

1 mgliquidVIMIZIM

HK 1 records · 1 strengths

Records without a stated strength · 1 VIMIZIM CONCENTRATE FOR SOLUTION FOR INFUSION 1MG/ML

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 VIMIZIM

Side-by-side table

Strength / form / release	US	GB	CA	AU	HK	EU
5 mg/5 mL injection	VIMIZIM	Vimizim 5mg/5ml concentrate for solution for infusion vials Vimizim 5mg/5ml solution for infusion vials	not recorded	not recorded	not recorded	not recorded
1 mg liquid	not recorded	not recorded	VIMIZIM	not recorded	not recorded	not recorded
1 mg/mL injection	not recorded	not recorded	not recorded	VIMIZIM elosulfase alfa (rch) 1 mg/mL concentrated solution for injection vial	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	VIMIZIM	VIMIZIM CONCENTRATE FOR SOLUTION FOR INFUSION 1MG/ML	VIMIZIM

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

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