Regorafenib
ATC L01EX05 · 10 markets · 22 records
CN 11 records · 1 strengths
- 40 mgtablet拜万戈瑞戈非尼__mah__:上海创诺制药有限公司、__mah__:南京正大天晴制药有限公司、__mah__:扬子江药业集团有限公司、__mah__:江西科睿药业有限公司、__mah__:湖南明瑞制药股份有限公司、__mah__:湖南科伦制药有限公司、__mah__:石药集团欧意药业有限公司、__mah__:重庆药友制药有限责任公司 +1
GB 2 records · 1 strengths
- 40 mgtabletStivarga
AU 2 records · 2 strengths
- 40 mgtabletSTIVARGA regorafenib 40 mg tablet bottle
Records without a stated strength · 1 Stivarga
US 1 records · 1 strengths
- 40 mgtabletStivarga
CA 1 records · 1 strengths
- 40 mgtabletStivarga
SG 1 records · 1 strengths
- 40 mgtabletStivarga
ES 1 records · 1 strengths
- 40 mgtabletStivarga
TW 1 records · 1 strengths
- 40 mgtabletStivarga癌瑞格膜衣錠40毫克
HK 1 records · 1 strengths
Records without a stated strength · 1 Stivarga
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 Stivarga
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 40 mg tablet | Stivarga | Stivarga | Stivarga | STIVARGA regorafenib 40 mg tablet bottle | Stivarga | Manufacturer: 上海创诺制药有限公司 Manufacturer: 南京正大天晴制药有限公司 Manufacturer: 扬子江药业集团有限公司+7Manufacturer: 江西科睿药业有限公司 ×2 Manufacturer: 湖南明瑞制药股份有限公司 Manufacturer: 湖南科伦制药有限公司 Manufacturer: 石药集团欧意药业有限公司 Manufacturer: 重庆药友制药有限责任公司 Manufacturer: 齐鲁制药有限公司 拜万戈瑞戈非尼 | Stivarga | Stivarga 癌瑞格膜衣錠40毫克 | ||
unknown | Stivarga | Stivarga | Stivarga |
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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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.