Vismodegib

ATC L01XJ01 · 9 markets · 12 records

Vismodegib 9 markets · 12 records Forms

AU 3 records · 2 strengths

150 mgcapsuleERIVEDGE+1ERIVEDGE vismodegib 150 mg hard capsule bottle also in CA·US·GB +3 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ERIVEDGE ×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

CA 2 records · 1 strengths

150 mgcapsuleERIVEDGE+1SPC-VISMODEGIB also in AU·US·GB +3

US 1 records · 1 strengths

150 mgcapsuleERIVEDGE also in AU·CA·GB +3

GB 1 records · 1 strengths

150 mgcapsuleERIVEDGE also in AU·CA·US +3

ES 1 records · 1 strengths

150 mgcapsuleERIVEDGE also in AU·CA·US +3

TW 1 records · 1 strengths

150 mgcapsuleERIVEDGE+1愛維德膠囊150毫克 also in AU·CA·US +3

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ERIVEDGE ×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

FR 1 records · 1 strengths

150 mgcapsuleERIVEDGE 150 mg, gélule also in AU·CA·US +3

Side-by-side table

Strength / form / release	US	GB	CA	AU	ES	TW	EU	FR
150 mg capsule	ERIVEDGE	ERIVEDGE	ERIVEDGE SPC-VISMODEGIB	ERIVEDGE ERIVEDGE vismodegib 150 mg hard capsule bottle	ERIVEDGE	ERIVEDGE 愛維德膠囊150毫克	not recorded	ERIVEDGE 150 mg, gélule
not disclosed unknown	not recorded	not recorded	not recorded	ERIVEDGE	not recorded	not recorded	ERIVEDGE	not recorded

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

“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.