Mirikizumab

Records for this ingredient, by country (identity only).

ATC L04AC24 · 9 markets · 36 records

Mirikizumab 9 markets · 36 records Forms
Filters

CA 7 records · 4 shown of 4 Source Health Canada Drug Product Databas · Data as of 2026-10-23

  • 100 mg per mL / per unit basis not statedliquidOmvoh
  • 100 mg/1 mLliquidOmvoh
  • 100 mL/1 mLliquidOmvoh
  • 20 mg per mL / per unit basis not statedliquidOmvoh

AU 7 records · 2 shown of 2 Source TGA · Data as of 2026-10-28 · includes records with unknown status (not proof of sale)

  • 100 mg/mL per mL / per unit basis not statedinjectionOMVOH mirikizumab 100 mg/mL + 200 mg/2 mL solution for injection autoinjector (pre-filled pen) composite pack (citrate-free formulation)OMVOH mirikizumab 100 mg/mL + 200 mg/2 mL solution for injection pre-filled syringe (composite pack) (citrate free formulation)、OMVOH mirikizumab 100 mg/mL solution for injection autoinjector (pre-filled pen)、OMVOH mirikizumab 100 mg/mL solution for injection autoinjector (pre-filled pen) (citrate-free formulation)、OMVOH mirikizumab 100 mg/mL solution for injection pre-filled syringe、OMVOH mirikizumab 100 mg/mL solution for injection pre-filled syringe (citrate-free formulation) unknown
  • 20 mg/mL per mL / per unit basis not statedinjectionOMVOH mirikizumab 300 mg/15 mL (20 mg/mL) concentrated injection vial for IV infusion unknown

US 5 records · 2 shown of 2 Source openFDA NDC Directory · Data as of 2026-10-23

  • 100 mg per mL / per unit basis not statedinjectionOmvoh
  • 20 mg per mL / per unit basis not statedinjectionOmvoh

JP 5 records · 3 shown of 3 Source 厚生労働省 薬価基準収載品目リスト · Data as of 2026-11-01

  • 100 mg/1 mLinjectionオンボー皮下注100mgオートインジェクターオンボー皮下注100mgシリンジ also in GB
  • 200 mg/2 mLinjectionオンボー皮下注200mgオートインジェクターオンボー皮下注200mgシリンジ also in GB
  • 300 mg/15 mLinjectionオンボー点滴静注300mg also in GB

GB 4 records · 3 shown of 3 Source NHSBSA dm+d · Data as of 2026-10-19

ES 3 records · 3 shown of 3 Source CIMA (AEMPS) · Data as of live

TW 2 records · 2 shown of 2 Source 衛生福利部食品藥物管理署(TFDA)全部藥品許可證資料集 · Data as of 2026-10-22

MX 1 records · 0 shown of 0 Source COFEPRIS · Data as of annual · some records have no stated strength

1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商

EU 1 records · 0 shown of 0 Source European Commission · Data as of 2026-11-03 · some records have no stated strength

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.

1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商

Some strengths are recorded without a per mL / per unit basis. They are shown as recorded and are not compared with other markets.

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.

A side-by-side table is offered only when this ingredient has records in many markets; otherwise this list is the whole picture.