Ramucirumab
ATC L01FG02 · 10 markets · 21 records
GB 4 records · 2 strengths
- 500 mg/50 mLinjectionCyramza 500mg/50ml concentrate for solution for infusion vials
- 100 mg/10 mLinjectionCyramza 500mg/50ml concentrate for solution for infusion vials
ES 4 records · 1 strengths
- 10 mg/1 mLinjectionCYRAMZA
US 2 records · 1 strengths
- 10 mgliquidCYRAMZA
SG 2 records · 1 strengths
- 10 mg/mLinjectionCYRAMZA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML
CN 2 records · 2 strengths
CA 1 records · 1 strengths
- 10 mgliquidCYRAMZA
TW 1 records · 1 strengths
Records without a stated strength · 1 CYRAMZA、欣銳擇 注射劑
HK 1 records · 1 strengths
Records without a stated strength · 1 CYRAMZA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML
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 CYRAMZA
| Strength / form / release | US | GB | CA | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 10 mg liquid | CYRAMZA | CYRAMZA | |||||||
| 500 mg/50 mL injection | Cyramza 500mg/50ml concentrate for solution for infusion vials | 希冉择雷莫西尤单抗 | |||||||
| 100 mg/10 mL injection | Cyramza 500mg/50ml concentrate for solution for infusion vials | 希冉择雷莫西尤单抗 | |||||||
| 10 mg/1 mL injection | CYRAMZA | ||||||||
| 10 mg/mL injection | CYRAMZA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML | ||||||||
injection | CYRAMZA 欣銳擇 注射劑 | ||||||||
unknown | CYRAMZA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML | CYRAMZA |
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Each country column shows the locally registered trade names — not translations.
4 more strength/form rows are recorded only in SG · ES · TW · HK · EU and are not shown in this table. Hay 4 filas de concentración/forma registradas solo en SG · ES · TW · HK · EU que no se muestran en esta tabla. 另有 4 个规格/剂型仅在 SG · ES · TW · HK · EU 有记录(未在本表显示)。 另有 4 個規格/劑型僅在 SG · ES · TW · HK · EU 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.
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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.