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Plasma-Lyte 148

The George Institute · FDA-approved active Small molecule Quality 2/100

Plasma-Lyte 148 is a marketed solution developed by The George Institute, currently holding a position in the electrolyte and fluid replacement market. A key strength of Plasma-Lyte 148 is its key composition patent, which is set to expire in 2028, providing a period of exclusive market protection. The primary risk facing Plasma-Lyte 148 is the potential increase in competition post-patent expiry in 2028.

At a glance

Generic namePlasma-Lyte 148
Also known asBalanced multi-electrolyte solution, Balanced crystalloid solution
SponsorThe George Institute
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

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