Pegcetacoplan

ATC L04AJ03 · 6 markets · 12 records

Pegcetacoplan 6 markets · 12 records Forms

AU 5 records · 4 strengths

1,080 mg/20 mLinjectionEmpaveli also in US·GB
1,080 mginjectionEMPAVELI pegcetacoplan 1080 mg/20 mL injection solution vial also in ES unknown
15 mginjectionSYFOVRE pegcetacoplan 15 mg/0.1 mL solution for injection vial unknown

Records without a stated strength · 1 Empaveli、Syfovre

US 2 records · 2 strengths

1,080 mg/20 mLinjectionEmpaveli also in AU·GB
15 mg/0.1 mLinjectionSyfovre

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 ASPAVELI、Syfovre

GB 1 records · 1 strengths

1,080 mg/20 mLinjectionAspaveli 1080mg/20ml solution for infusion vials also in AU·US

CA 1 records · 1 strengths

54 mg/1 mLliquidEmpaveli

ES 1 records · 1 strengths

1,080 mginjectionASPAVELI also in AU

Side-by-side table

Strength / form / release	US	GB	CA	AU	ES	EU
1,080 mg/20 mLRecorded as: 1.08 g/20 mL injection	Empaveli	Aspaveli 1080mg/20ml solution for infusion vials	not recorded	Empaveli	not recorded	not recorded
1,080 mg injection	not recorded	not recorded	not recorded	EMPAVELI pegcetacoplan 1080 mg/20 mL injection solution vial	ASPAVELI	not recorded
54 mg/1 mL liquid	not recorded	not recorded	Empaveli	not recorded	not recorded	not recorded
15 mg/0.1 mL injection	Syfovre	not recorded	not recorded	not recorded	not recorded	not recorded
15 mg injection	not recorded	not recorded	not recorded	SYFOVRE pegcetacoplan 15 mg/0.1 mL solution for injection vial	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	Empaveli Syfovre	not recorded	ASPAVELI Syfovre

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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.