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Piperacillin-tazobactam administered in a standard infusion

CR-CSSS Champlain-Charles-Le Moyne · FDA-approved active Small molecule Quality 5/100

Piperacillin-tazobactam administered in a standard infusion is a Small molecule drug developed by CR-CSSS Champlain-Charles-Le Moyne. It is currently FDA-approved.

Piperacillin-tazobactam, marketed by CR-CSSS Champlain-Charles-Le Moyne, is a well-established antibiotic combination used for treating a variety of bacterial infections. The key composition patent is set to expire in 2028, providing a period of market exclusivity and potential revenue stability. However, the primary risk lies in the potential increase in generic competition following the patent expiry, which could significantly impact market share and revenue.

At a glance

Generic namePiperacillin-tazobactam administered in a standard infusion
SponsorCR-CSSS Champlain-Charles-Le Moyne
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

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Frequently asked questions about Piperacillin-tazobactam administered in a standard infusion

What is Piperacillin-tazobactam administered in a standard infusion?

Piperacillin-tazobactam administered in a standard infusion is a Small molecule drug developed by CR-CSSS Champlain-Charles-Le Moyne.

Who makes Piperacillin-tazobactam administered in a standard infusion?

Piperacillin-tazobactam administered in a standard infusion is developed and marketed by CR-CSSS Champlain-Charles-Le Moyne (see full CR-CSSS Champlain-Charles-Le Moyne pipeline at /company/cr-csss-champlain-charles-le-moyne).

What development phase is Piperacillin-tazobactam administered in a standard infusion in?

Piperacillin-tazobactam administered in a standard infusion is FDA-approved (marketed).

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