Brodalumab

ATC L04AC12 · 7 markets · 7 records

Brodalumab 7 markets · 7 records Forms

US 1 records · 1 strengths

210 mginjectionSiliq also in ES·TW

GB 1 records · 1 strengths

210 mg/1.5 mLinjectionKyntheum 210mg/1.5ml solution for injection pre-filled syringes

CA 1 records · 1 strengths

140 mg/1 mLliquidSiliq

ES 1 records · 1 strengths

210 mginjectionKYNTHEUM PRECARGADA also in US·TW

TW 1 records · 1 strengths

210 mginjectionLUMICEF Subcutaneous Injection 210mg Syringe+1立美西膚皮下注射劑210毫克 also in US·ES

HK 1 records · 1 strengths

Records without a stated strength · 1 LUMICEF SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 210MG/1.5ML

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 Kyntheum

Side-by-side table

Strength / form / release	US	GB	CA	ES	TW	HK	EU
210 mg injection	Siliq	not recorded	not recorded	KYNTHEUM PRECARGADA	LUMICEF Subcutaneous Injection 210mg Syringe 立美西膚皮下注射劑210毫克	not recorded	not recorded
140 mg/1 mL liquid	not recorded	not recorded	Siliq	not recorded	not recorded	not recorded	not recorded
210 mg/1.5 mL injection	not recorded	Kyntheum 210mg/1.5ml solution for injection pre-filled syringes	not recorded	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	not recorded	not recorded	LUMICEF SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 210MG/1.5ML	Kyntheum

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

2 more strength/form rows are recorded only in GB · HK · EU and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en GB · HK · EU que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 GB · HK · EU 有记录（未在本表显示）。另有 2 個規格/劑型僅在 GB · HK · EU 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.

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.