Enmetazobactam

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

ATC — · 3 markets · 3 records

Enmetazobactam 3 markets · 3 records Forms

Filters

MarketGB 1 ES 1 EU 1

Kind

Strength

GB 1 records · 1 shown of 1 Source NHSBSA dm+d · Data as of 2026-10-19

Combination products containing this ingredient

500 mg per mL / per unit basis not statedinjection CombinationCefepime 2,000 mg + Enmetazobactam 500 mgExblifep 2g/0.5g powder for concentrate for solution for infusion vials

ES 1 records · 1 shown of 1 Source CIMA (AEMPS) · Data as of live

Combination products containing this ingredient

500 mg per mL / per unit basis not statedinjection CombinationCefepime 2,000 mg + Enmetazobactam 500 mgEXBLIFEP

EU 1 records · 0 shown of 0 Source European Commission · Data as of 2026-11-03 · some records have no stated strength

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EXBLIFEP ×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	GB	ES	EU
500 mgRecorded as: 0.5 g per mL / per unit basis not stated cannot compare Combination Cefepime 2,000 mg + Enmetazobactam 500 mg injection	Exblifep 2g/0.5g powder for concentrate for solution for infusion vials	EXBLIFEP	not recorded
not disclosed Combination Cefepime + Enmetazobactam unknown	not recorded	not recorded	EXBLIFEP

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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.