Vutrisiran

ATC N07XX18 · 10 markets · 14 records

Vutrisiran 10 markets · 14 records Forms

AU 3 records · 3 strengths

25 mg/0.5 mLinjectionAMVUTTRA also in US·GB
26.5 mginjectionAMVUTTRA, vutrisiran (as sodium) 25 mg / 0.5 mL solution for injection pre-filled syringe 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AMVUTTRA ×4

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

TW 2 records · 1 strengths

2 records · 0 manufacturers 2 registros · 0 fabricantes 2 个记录 · 0 个厂家 2 個記錄 · 0 個廠商

With a brand name Con nombre comercial 有商品名有商品名Amvuttra Solution for injection in pre-filled syringe ×6安步達預充填式注射劑 ×1恩賦翠預充填式注射劑 ×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 strengths

25 mg/0.5 mLinjectionAMVUTTRA also in AU·GB

GB 1 records · 1 strengths

25 mg/0.5 mLinjectionAmvuttra 25mg/0.5ml solution for injection pre-filled syringes also in AU·US

CA 1 records · 1 strengths

25 mgliquidAMVUTTRA

SG 1 records · 1 strengths

25 mginjectionAmvuttra Solution for injection in pre-filled syringe also in ES·FR

ES 1 records · 1 strengths

25 mginjectionAMVUTTRA PRECARGADA also in SG·FR

HK 1 records · 1 strengths

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Amvuttra Solution for injection in pre-filled syringe ×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

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.

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AMVUTTRA ×2

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

FR 1 records · 1 strengths

25 mginjectionAMVUTTRA 25 mg, solution injectable en seringue préremplie also in SG·ES

Side-by-side table

Strength / form / release	US	GB	CA	AU	SG	ES	TW	HK	EU	FR
25 mg/0.5 mL injection	AMVUTTRA	Amvuttra 25mg/0.5ml solution for injection pre-filled syringes	not recorded	AMVUTTRA	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
25 mg injection	not recorded	not recorded	not recorded	not recorded	Amvuttra Solution for injection in pre-filled syringe	AMVUTTRA PRECARGADA	not recorded	not recorded	not recorded	AMVUTTRA 25 mg, solution injectable en seringue préremplie
25 mg liquid	not recorded	not recorded	AMVUTTRA	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
26.5 mg injection	not recorded	not recorded	not recorded	AMVUTTRA, vutrisiran (as sodium) 25 mg / 0.5 mL solution for injection pre-filled syringe	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
not disclosed injection	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	Amvuttra Solution for injection in pre-filled syringe 安步達預充填式注射劑恩賦翠預充填式注射劑	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	AMVUTTRA	not recorded	not recorded	not recorded	Amvuttra Solution for injection in pre-filled syringe	AMVUTTRA	not recorded

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