Fampridine
ATC N07XX07 · 6 markets · 27 records
GB 6 records · 2 strengths
- 10 mgtablet · extended-releaseFampyra 10mg modified-release tablets__no_trade__
- 10 mgcapsule4-Aminopyridine 10mg capsules
CA 4 records · 1 strengths
- 10 mgtablet · extended-releaseAPO-FAMPRIDINEFAMPYRA、PMS-FAMPRIDINE、TARO-FAMPRIDINE
AU 4 records · 2 strengths
- 10 mgtablet · extended-releaseAPO-FAMPRIDINE MR fampridine 10mg modified release tablets blister packFAMPRIDINE MR APOTEX fampridine 10mg modified release tablets blister pack、FAMPYRA fampridine 10mg modified release tablets bottle
Records without a stated strength · 1 FAMPYRA
ES 4 records · 1 strengths
- 10 mgtablet · extended-releaseFAMPRIDINA ACCORDFAMPRIDINA AUROVITAS、FAMPRIDINA STADA、FAMPYRA
EU 2 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 Fampridine Accord、FAMPYRA
MX 1 records · 1 strengths
Records without a stated strength · 1 FAMPYRA
| Strength / form / release | GB | CA | AU | ES | MX | EU |
|---|---|---|---|---|---|---|
| 10 mg tablet · extended-release | No trade name Fampyra 10mg modified-release tablets | APO-FAMPRIDINE FAMPYRA PMS-FAMPRIDINE+1TARO-FAMPRIDINE | APO-FAMPRIDINE MR fampridine 10mg modified release tablets blister pack FAMPRIDINE MR APOTEX fampridine 10mg modified release tablets blister pack FAMPYRA fampridine 10mg modified release tablets bottle | FAMPRIDINA ACCORD FAMPRIDINA AUROVITAS FAMPRIDINA STADA+1FAMPYRA | ||
| 10 mg capsule | 4-Aminopyridine 10mg capsules | |||||
unknown | FAMPYRA | Fampridine Accord FAMPYRA | ||||
tablet | FAMPYRA |
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Each country column shows the locally registered trade names — not translations.
2 more strength/form rows are recorded only in GB · MX and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en GB · MX que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 GB · MX 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 GB · MX 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.