Diroximel
ATC — · 7 markets · 9 records
AU 3 records · 2 strengths
- 231 mgcapsule · delayed-releaseVumerityVUMERITY diroximel fumarate 231 mg enteric capsules 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
US 1 records · 1 strengths
- 231 mgcapsuleVumerity
GB 1 records · 1 strengths
- 231 mgcapsule · delayed-releaseVumerity 231mg gastro-resistant capsules
ES 1 records · 1 strengths
- 231 mgcapsule · delayed-releaseVumerity
MX 1 records · 1 strengths
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
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.
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 1 records · 1 strengths
- 231 mgtablet · delayed-releaseVUMERITY 231 mg, gélule gastro-résistante
| Strength / form / release | US | GB | AU | ES | MX | EU | FR |
|---|---|---|---|---|---|---|---|
| 231 mg capsule · delayed-release | Vumerity 231mg gastro-resistant capsules | Vumerity VUMERITY diroximel fumarate 231 mg enteric capsules bottle | Vumerity | ||||
| 231 mg tablet · delayed-release | VUMERITY 231 mg, gélule gastro-résistante | ||||||
| 231 mg capsule | Vumerity | ||||||
unknown | Vumerity | Vumerity | |||||
capsule | Vumerity |
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Each country column shows the locally registered trade names — not translations.
2 more strength/form rows are recorded only in MX · FR and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en MX · FR que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 MX · FR 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 MX · 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Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.