Amifampridine
Records for this ingredient, by country (identity only).
ATC N07XX05 · 7 markets · 18 records
GB 6 records · 2 shown of 2
- 10 mgtablet3,4-Diaminopyridine 20mg tabletsFirdapse、Manufacturer: Lupin Healthcare (UK) Ltd、Manufacturer: Special Order
- 20 mgtablet3,4-Diaminopyridine 20mg tabletsManufacturer: Special Order
AU 3 records · 1 shown of 1
- 10 mgtabletRuzurgiRUZURGI amifampridine 10 mg tablet bottle
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
FR 3 records · 2 shown of 2
- 10 mgtabletAMIFAMPRIDINE SERB 10 mg, compriméAMIFAMPRIDINE SUBSTIPHARM 10 mg, comprimé sécable
- 18.98 mgtabletFIRDAPSE 10 mg, comprimé
CA 2 records · 1 shown of 1
- 10 mgtabletFirdapseRuzurgi
EU 2 records · 0 shown of 0
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.
2 records · 0 manufacturers 2 registros · 0 fabricantes 2 个记录 · 0 个厂家 2 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
US 1 records · 1 shown of 1
- 10 mgtabletFirdapse
JP 1 records · 1 shown of 1
- 10 mgtabletファダプス錠10mg
| Strength / form / release | US | GB | CA | AU | JP | EU | FR |
|---|---|---|---|---|---|---|---|
| 10 mg tablet | Firdapse | 3,4-Diaminopyridine 20mg tablets Manufacturer: Lupin Healthcare (UK) Ltd Manufacturer: Special Order ×2+1Firdapse | Firdapse Ruzurgi | Ruzurgi RUZURGI amifampridine 10 mg tablet bottle | ファダプス錠10mg | AMIFAMPRIDINE SERB 10 mg, comprimé AMIFAMPRIDINE SUBSTIPHARM 10 mg, comprimé sécable | |
| 20 mg tablet | 3,4-Diaminopyridine 20mg tablets Manufacturer: Special Order ×2 | ||||||
| 18.98 mg tablet | FIRDAPSE 10 mg, comprimé | ||||||
unknown | Ruzurgi | Amifampridine SERB Firdapse |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in FR and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en FR que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 FR 有记录（未在本表显示）。 另有 1 個規格/劑型僅在 FR 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.
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.