Relebactam

ATC — · 7 markets · 7 records

Relebactam 7 markets · 7 records Forms

Filters

MarketUS 1 GB 1 CA 1 ES 1 TW 1 EU 1 FR 1

Kind

Strength

US 1 records · 1 shown of 1 Source openFDA NDC Directory · Data as of 2026-10-23

Combination products containing this ingredient

250 mg/100 mLinjection CombinationCilastatin 500 mg/100 mL + Imipenem 500 mg/100 mL + Relebactam 250 mg/100 mLRECARBRIO

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

Combination products containing this ingredient

250 mginjection CombinationCilastatin 500 mg + Imipenem 500 mg + Relebactam 250 mgRecarbrio 500mg/500mg/250mg powder for solution for infusion vials also in ES

CA 1 records · 1 shown of 1 Source Health Canada Drug Product Databas · Data as of 2026-10-23

Combination products containing this ingredient

250 mgpowder CombinationCilastatin 500 mg + Imipenem 500 mg + Relebactam 250 mgRECARBRIO

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

Combination products containing this ingredient

250 mginjection CombinationCilastatin 500 mg + Imipenem 500 mg + Relebactam 250 mgRECARBRIO also in GB

TW 1 records · 0 shown of 0 Source 衛生福利部食品藥物管理署（TFDA）全部藥品許可證資料集 · Data as of 2026-10-22 · some records have no stated strength

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RECARBRIO Powder for solution for infusion ×1瑞必優乾粉注射劑 ×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

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RECARBRIO ×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

FR 1 records · 0 shown of 0 Source Base de données publique des médic · Data as of 2026-11-03 · some records have no stated strength

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RECARBRIO 500 mg/500 mg/250 mg, poudre pour solution pour perfusion ×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

Side-by-side table

Strength / form / release	US	GB	CA	ES	TW	EU	FR
250 mg Combination Cilastatin 500 mg + Imipenem 500 mg + Relebactam 250 mg injection	not recorded	Recarbrio 500mg/500mg/250mg powder for solution for infusion vials	not recorded	RECARBRIO	not recorded	not recorded	not recorded
250 mg/100 mL Combination Cilastatin 500 mg/100 mL + Imipenem 500 mg/100 mL + Relebactam 250 mg/100 mL injection	RECARBRIO	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
250 mg Combination Cilastatin 500 mg + Imipenem 500 mg + Relebactam 250 mg powder	not recorded	not recorded	RECARBRIO	not recorded	not recorded	not recorded	not recorded
not disclosed Combination Cilastatin + Imipenem + Relebactam injection	not recorded	not recorded	not recorded	not recorded	RECARBRIO Powder for solution for infusion 瑞必優乾粉注射劑	not recorded	RECARBRIO 500 mg/500 mg/250 mg, poudre pour solution pour perfusion
not disclosed Combination Cilastatin + Imipenem + Relebactam unknown	not recorded	not recorded	not recorded	not recorded	not recorded	RECARBRIO	not recorded

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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 · ES · EU and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en GB · ES · EU que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 GB · ES · EU 有记录（未在本表显示）。另有 2 個規格/劑型僅在 GB · ES · 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.