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Piperacillin Sodium and Sulbactam Sodium

Xiangbei Welman Pharmaceutical Co., Ltd · FDA-approved active Small molecule

Piperacillin inhibits bacterial cell wall synthesis by binding penicillin-binding proteins, while sulbactam inhibits bacterial β-lactamases to prevent antibiotic degradation.

Piperacillin inhibits bacterial cell wall synthesis by binding penicillin-binding proteins, while sulbactam inhibits bacterial β-lactamases to prevent antibiotic degradation. Used for Bacterial infections caused by susceptible organisms including intra-abdominal infections, gynecological infections, skin and soft tissue infections, and respiratory tract infections, Polymicrobial infections and infections caused by β-lactamase-producing bacteria.

At a glance

Generic namePiperacillin Sodium and Sulbactam Sodium
Also known asxin te mie, te mie jun, xin ke jun
SponsorXiangbei Welman Pharmaceutical Co., Ltd
Drug classβ-lactam antibiotic with β-lactamase inhibitor
TargetPenicillin-binding proteins; bacterial β-lactamases
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Piperacillin is a broad-spectrum β-lactam antibiotic that disrupts peptidoglycan cross-linking in bacterial cell walls, leading to cell lysis and death. Sulbactam is a β-lactamase inhibitor that protects piperacillin from enzymatic degradation by resistant bacteria, extending the spectrum of activity against β-lactamase-producing organisms. Together, this combination provides enhanced coverage against gram-positive, gram-negative, and anaerobic bacteria.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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