Darolutamide

ATC L02BB06 · 10 markets · 13 records

Darolutamide 10 markets · 13 records Forms

AU 4 records · 2 strengths

300 mgtabletNUBEQA+2NUBEQA darolutamide 300 mg tablet blister pack、NUBEQA darolutamide 300 mg tablet bottle also in US·GB·CA +4 unknown

Records without a stated strength · 1 NUBEQA

US 1 records · 1 strengths

300 mgtabletNUBEQA also in AU·GB·CA +4

GB 1 records · 1 strengths

300 mgtabletNUBEQA also in AU·US·CA +4

CA 1 records · 1 strengths

300 mgtabletNUBEQA also in AU·US·GB +4

SG 1 records · 1 strengths

300 mgtabletNUBEQA also in AU·US·GB +4

ES 1 records · 1 strengths

300 mgtabletNUBEQA also in AU·US·GB +4

MX 1 records · 1 strengths

300 mgtabletNUBEQAL also in AU·US·GB +4

TW 1 records · 1 strengths

300 mgtabletNUBEQA F.C. Tablets 300 mg+1諾博戈膜衣錠300毫克 also in AU·US·GB +4

HK 1 records · 1 strengths

Records without a stated strength · 1 NUBEQA

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 NUBEQA

Side-by-side table

Strength / form / release	US	GB	CA	AU	SG	ES	MX	TW	HK	EU
300 mg tablet	NUBEQA	NUBEQA	NUBEQA	NUBEQA NUBEQA darolutamide 300 mg tablet blister pack NUBEQA darolutamide 300 mg tablet bottle	NUBEQA	NUBEQA	NUBEQAL	NUBEQA F.C. Tablets 300 mg 諾博戈膜衣錠300毫克	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	NUBEQA	not recorded	not recorded	not recorded	not recorded	NUBEQA	NUBEQA

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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.