Eteplirsen

Records for this ingredient, by country (identity only).

ATC M09AX06 · 3 markets · 7 records

Eteplirsen 3 markets · 7 records Forms

Filters

MarketUS 4 GB 2 EU 1

Strength

US 4 records · 3 shown of 3 Source openFDA NDC Directory · Data as of 2026-10-23

500 mg/10 mLinjectionManufacturer: Catalent Indiana, LLC ×2 also in GB
100 mg/2 mLinjectionManufacturer: Catalent Indiana, LLC ×2 also in GB
50 mg per mL / per unit basis not statedinjectionExondys 51

GB 2 records · 2 shown of 2 Source NHSBSA dm+d · Data as of 2026-10-19

500 mg/10 mLinjectionExondys 51 100mg/2ml solution for injection vials also in US
100 mg/2 mLinjectionExondys 51 100mg/2ml solution for injection vials also in US

EU 1 records · 0 shown of 0 Source European Commission · Data as of 2026-11-03 · some records have no stated strength · includes records with unknown status (not proof of sale)

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Exondys ×1

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

Some strengths are recorded without a per mL / per unit basis. They are shown as recorded and are not compared with other markets.

Side-by-side table

Strength / form / release	US	GB	EU
500 mg/10 mL injection	Manufacturer: Catalent Indiana, LLC ×2	Exondys 51 100mg/2ml solution for injection vials	not recorded
100 mg/2 mL injection	Manufacturer: Catalent Indiana, LLC ×2	Exondys 51 100mg/2ml solution for injection vials	not recorded
50 mg per mL / per unit basis not stated cannot compare injection	Exondys 51	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	Exondys

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

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

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.