Obinutuzumab
ATC L01FA03 · 10 markets · 14 records
AU 3 records · 3 strengths
- 1,000 mg/40 mLinjectionGazyva
- 1,000 mginjectionGAZYVA obinutuzumab (rch) 1000 mg/40 mL concentrate solution for infusion vial
Records without a stated strength · 1 Gazyva
GB 2 records · 1 strengths
- 1,000 mg/40 mLinjectionGazyvaro 1000mg/40ml concentrate for solution for infusion vials
ES 2 records · 1 strengths
- 1,000 mginjectionGAZYVARO
US 1 records · 1 strengths
- 1,000 mg/40 mLinjectionGazyva
CA 1 records · 1 strengths
- 25 mgliquidGazyva
SG 1 records · 1 strengths
- 1,000 mg/40 mLinjectionGAZYVA CONCENTRATE FOR SOLUTION FOR INFUSION 1000MG/40ML
CN 1 records · 1 strengths
- 1,000 mginjection佳罗华奥妥珠单抗
TW 1 records · 1 strengths
Records without a stated strength · 1 Gazyva solution for infusion、癌即瓦注射劑
HK 1 records · 1 strengths
Records without a stated strength · 1 GAZYVA CONCENTRATE FOR SOLUTION FOR INFUSION 1000MG/40ML
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 GAZYVARO
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 1,000 mg/40 mLRecorded as: 1 g/40 mL injection | Gazyva | Gazyvaro 1000mg/40ml concentrate for solution for infusion vials | Gazyva | GAZYVA CONCENTRATE FOR SOLUTION FOR INFUSION 1000MG/40ML | ||||||
| 1,000 mg injection | GAZYVA obinutuzumab (rch) 1000 mg/40 mL concentrate solution for infusion vial | 佳罗华奥妥珠单抗 | GAZYVARO | |||||||
| 25 mg liquid | Gazyva | |||||||||
unknown | Gazyva | GAZYVA CONCENTRATE FOR SOLUTION FOR INFUSION 1000MG/40ML | GAZYVARO | |||||||
injection | Gazyva solution for infusion 癌即瓦注射劑 |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in CA and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en CA que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 CA 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 CA 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.