This brand name is authorized in Austria, Estonia, Finland, France, Croatia, Ireland, Italy, Japan, Lithuania, Netherlands, Romania, United Kingdom, United States
The drug RECARBRIO contains a combination of these active pharmaceutical ingredients (APIs):
1
Imipemide
UNII Q20IM7HE75 - IMIPENEM ANHYDROUS
|
Imipenem is a semi-synthetic derivative of thienamycin, the parent compound produced by the filamentous bacterium Streptomyces cattleya. Imipenem exerts its bactericidal activity by inhibiting bacterial cell wall synthesis in Gram-positive and Gram-negative bacteria through binding to penicillin-binding proteins (PBPs). |
2
Cilastatin
UNII 141A6AMN38 - CILASTATIN
|
|
3
Relebactam
UNII 1OQF7TT3PF - RELEBACTAM ANHYDROUS
|
Relebactam is a non-beta lactam inhibitor of Ambler class A and class C beta-lactamases, including class A Klebsiella pneumoniae carbapenemase (KPC) and extended-spectrum beta-lactamases (ESBLs), and class C (AmpC-type) beta-lactamases including Pseudomonas-Derived Cephalosporinase (PDC). Relebactam does not inhibit class B enzymes (metallo-beta-lactamases) or class D carbapenemases. Relebactam has no antibacterial activity. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
RECARBRIO Powder for solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
RECARBRIO Powder for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
J01DH56 | J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01D Other beta-lactam antibacterials → J01DH Carbapenems | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: EE | Ravimiamet | Identifier(s): 1811359 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 070677 |
Country: FR | Base de données publique des médicaments | Identifier(s): 65172663 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 386996 |
Country: IT | Agenzia del Farmaco | Identifier(s): 048537017 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 6129500D1027 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1089413 |
Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 203068 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W66566001 |
Country: US | FDA, National Drug Code | Identifier(s): 0006-3856 |
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