Fenfluramine

ATC N03AX26 · 8 markets · 9 records

Fenfluramine 8 markets · 9 records Forms

US 1 records · 1 strengths

2.2 mgliquidFintepla also in GB·TW

GB 1 records · 1 strengths

2.2 mgliquidFintepla 2.2mg/ml oral solution also in US·TW

AU 1 records · 1 strengths

2.2 mg/1 mLliquidFintepla also in ES

ES 1 records · 1 strengths

2.2 mg/1 mLliquidFintepla also in AU

TW 1 records · 1 strengths

2.2 mgliquidFintepla 2.2mg/ml oral solution+1飛癲寧口服溶液2.2毫克/毫升 also in US·GB

HK 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

With a brand name Con nombre comercial 有商品名有商品名Fintepla 2.2mg/ml oral solution ×3

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

With a brand name Con nombre comercial 有商品名有商品名Fintepla ×2

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

Side-by-side table

Strength / form / release	US	GB	AU	ES	TW	HK	EU
2.2 mg liquid	Fintepla	Fintepla 2.2mg/ml oral solution	not recorded	not recorded	Fintepla 2.2mg/ml oral solution 飛癲寧口服溶液2.2毫克/毫升	not recorded	not recorded
2.2 mg/1 mL liquid	not recorded	not recorded	Fintepla	Fintepla	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	not recorded	not recorded	Fintepla 2.2mg/ml oral solution	Fintepla

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Each country column shows the locally registered trade names — not translations.

1 more strength/form rows are recorded only in HK · EU and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en HK · EU que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 HK · EU 有记录（未在本表显示）。另有 1 個規格/劑型僅在 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.

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.

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The same ingredient can carry completely different brand names in different countries, and the same name can point to a different ingredient. Listed by country — not interchangeable.

Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.