Garadacimab
ATC B06AC07 · 7 markets · 11 records
AU 4 records · 3 strengths
- 200 mg/1.2 mLinjectionANDEMBRY
- 200 mginjectionANDEMBRY garadacimab 200 mg solution for injection pre-filled penANDEMBRY garadacimab 200 mg solution for injection pre-filled syringe with needle safety device
Records without a stated strength · 1 ANDEMBRY
CA 2 records · 1 strengths
- 166.666667 mg/1 mLliquidANDEMBRY
US 1 records · 1 strengths
- 200 mg/1.2 mLinjectionANDEMBRY
GB 1 records · 1 strengths
- 200 mg/1.2 mLinjectionAndembry 200mg/1.2ml solution for injection pre-filled pens
ES 1 records · 1 strengths
- 200 mginjectionANDEMBRY PRECARGADA
HK 1 records · 1 strengths
Records without a stated strength · 1 ANDEMBRY SOLUTION FOR INJECTION IN PRE-FILLED PEN 200MG/1.2ML
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 ANDEMBRY
| Strength / form / release | US | GB | CA | AU | ES | HK | EU |
|---|---|---|---|---|---|---|---|
| 200 mg/1.2 mL injection | ANDEMBRY | Andembry 200mg/1.2ml solution for injection pre-filled pens | ANDEMBRY | ||||
| 200 mg injection | ANDEMBRY garadacimab 200 mg solution for injection pre-filled pen ANDEMBRY garadacimab 200 mg solution for injection pre-filled syringe with needle safety device | ANDEMBRY PRECARGADA | |||||
| 166.666667 mg/1 mL liquid | ANDEMBRY | ||||||
unknown | ANDEMBRY | ANDEMBRY SOLUTION FOR INJECTION IN PRE-FILLED PEN 200MG/1.2ML | ANDEMBRY |
Scroll horizontally for more markets →
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.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.