Amivantamab

ATC L01FX18 · 11 markets · 35 records

Amivantamab 11 markets · 35 records Forms

AU 7 records · 7 strengths

  • 350 mginjectionRYBREVANT amivantamab 350 mg/7 mL concentrate for solution for infusion vial also in US·CN unknown
  • 350 mg/7 mLinjectionRybrevant also in GB·SG
  • 3,520 mginjectionRYBREVANT SC amivantamab 1600mg/10mL solution for injection vial also in ES unknown
  • 2,400 mginjectionRYBREVANT SC amivantamab 1600mg/10mL solution for injection vial also in ES unknown
  • 1,600 mginjectionRYBREVANT SC amivantamab 1600mg/10mL solution for injection vial also in ES unknown
  • 2,240 mginjectionRYBREVANT SC amivantamab 1600mg/10mL solution for injection vial unknown

Records without a stated strength · 1 Rybrevant

US 5 records · 5 strengths

GB 5 records · 5 strengths

CA 5 records · 2 strengths

ES 5 records · 5 strengths

MX 2 records · 1 strengths

    Records without a stated strength · 1 Rybrevant、Rybrevant Faspro

    TW 2 records · 2 strengths

    SG 1 records · 1 strengths

    CN 1 records · 1 strengths

    • 350 mginjection锐珂埃万妥单抗 also in AU·US

    HK 1 records · 1 strengths

      Records without a stated strength · 1 RYBREVANT CONCENTRATE FOR SOLUTION FOR INFUSION 350MG/7ML

      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 Rybrevant

        Side-by-side table

        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        Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.