Blinatumomab
ATC L01FX07 · 8 markets · 10 records
AU 3 records · 3 strengths
- 0.0385 mginjectionBLINCYTO
- 38.5 mcg/ginjectionBLINCYTO blinatumomab (rch) 38.5 microgram powder for injection vial with Intravenous (IV) solution stabiliser
Records without a stated strength · 1 BLINCYTO
GB 1 records · 1 strengths
Records without a stated strength · 1 Blincyto 38.5micrograms powder for concentrate and solution for solution for infusion vials
CA 1 records · 1 strengths
- 0.0385 mgpowderBLINCYTO
SG 1 records · 1 strengths
- 55 mcg/mLinjectionBLINCYTO POWDER FOR INFUSION 35 MCG/VIAL
ES 1 records · 1 strengths
- 0.0385 mginjectionBLINCYTO
TW 1 records · 1 strengths
Records without a stated strength · 1 BLINCYTO for Injection、百利妥注射劑
HK 1 records · 1 strengths
Records without a stated strength · 1 BLINCYTO POWDER FOR CONCENTRATE AND SOLUTION FOR SOLUTION FOR INFUSION 35MCG/VIAL
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 BLINCYTO
| Strength / form / release | GB | CA | AU | SG | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|
| 0.0385 mgRecorded as: 38.5 mcg、38.5 microgram injection | BLINCYTO | BLINCYTO | ||||||
| 55 mcg/mL injection | BLINCYTO POWDER FOR INFUSION 35 MCG/VIAL | |||||||
| 38.5 mcg/g injection | BLINCYTO blinatumomab (rch) 38.5 microgram powder for injection vial with Intravenous (IV) solution stabiliser | |||||||
| 0.0385 mgRecorded as: 38.5 mcg powder | BLINCYTO | |||||||
injection | Blincyto 38.5micrograms powder for concentrate and solution for solution for infusion vials | BLINCYTO for 百利妥注射劑 | ||||||
unknown | BLINCYTO | BLINCYTO POWDER FOR CONCENTRATE AND SOLUTION FOR SOLUTION FOR INFUSION 35MCG/VIAL | BLINCYTO |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in SG and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en SG que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 SG 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 SG 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.
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.