Belzutifan

ATC L01XX74 · 9 markets · 13 records

Belzutifan 9 markets · 13 records Forms

AU 4 records · 2 strengths

40 mgtabletWELIREG+2WELIREG belzutifan 40 mg film-coated tablet blister pack、WELIREG belzutifan 40 mg film-coated tablet bottle also in TW·US·GB +3 unknown

Records without a stated strength · 1 WELIREG

TW 2 records · 1 strengths

40 mgtabletWELIREG+3WELIREG-VHL 40 mg film-coated tablets、威立銳40毫克膜衣錠、威銳格40毫克膜衣錠 also in AU·US·GB +3

US 1 records · 1 strengths

40 mgtabletWELIREG also in AU·TW·GB +3

GB 1 records · 1 strengths

40 mgtabletWELIREG also in AU·TW·US +3

CA 1 records · 1 strengths

40 mgtabletWELIREG also in AU·TW·US +3

SG 1 records · 1 strengths

40 mgtabletWELIREG also in AU·TW·US +3

ES 1 records · 1 strengths

40 mgtabletWELIREG also in AU·TW·US +3

HK 1 records · 1 strengths

Records without a stated strength · 1 WELIREG

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 WELIREG

Side-by-side table

Strength / form / release	US	GB	CA	AU	SG	ES	TW	HK	EU
40 mg tablet	WELIREG	WELIREG	WELIREG	WELIREG WELIREG belzutifan 40 mg film-coated tablet blister pack WELIREG belzutifan 40 mg film-coated tablet bottle	WELIREG	WELIREG	WELIREG WELIREG-VHL 40 mg film-coated tablets 威立銳40毫克膜衣錠 +1 威銳格40毫克膜衣錠	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	WELIREG	not recorded	not recorded	not recorded	WELIREG	WELIREG

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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.

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.