Opicapone

ATC N04BX04 · 7 markets · 18 records

Opicapone 7 markets · 18 records Forms

ES 5 records · 1 strengths

50 mgcapsuleONGENTYS also in AU·US·GB +1

AU 3 records · 2 strengths

50 mgcapsuleONGENTYS+1ONGENTYS opicapone 50 mg hard capsule blister pack also in ES·US·GB +1 unknown

Records without a stated strength · 1 ONGENTYS

US 2 records · 2 strengths

50 mgcapsuleONGENTYS also in ES·AU·GB +1
25 mgcapsuleONGENTYS

GB 2 records · 1 strengths

50 mgcapsuleONGENTYS also in ES·AU·US +1

EU 2 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 ONGENTYS、Ontilyv

MX 1 records · 1 strengths

Records without a stated strength · 1 ONGENTYS

TW 1 records · 1 strengths

50 mgcapsuleOngentys 50mg Hard Capsules+1歐健體斯膠囊50毫克 also in ES·AU·US +1

Side-by-side table

Strength / form / release	US	GB	AU	ES	MX	TW	EU
50 mg capsule	ONGENTYS	ONGENTYS	ONGENTYS ONGENTYS opicapone 50 mg hard capsule blister pack	ONGENTYS	not recorded	Ongentys 50mg Hard Capsules 歐健體斯膠囊50毫克	not recorded
25 mg capsule	ONGENTYS	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	ONGENTYS	not recorded	not recorded	not recorded	ONGENTYS Ontilyv
not disclosed capsule	not recorded	not recorded	not recorded	not recorded	ONGENTYS	not recorded	not recorded

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

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