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Ketalar (ketamine)

Ph Health · FDA-approved active Verified Quality 75/100

Ketamine works by blocking the action of glutamate at the NMDA receptor, which is involved in pain perception and memory formation.

Ketalar (ketamine) is a general anesthetic drug that targets the glutamate NMDA receptor. Originally developed by PAR STERILE PRODUCTS and currently owned by Ph Health, it was FDA-approved in 1970 for general and local anesthesia. As an off-patent medication with multiple generic manufacturers, ketamine is widely available. Key safety considerations include its potential for abuse and dependence. Its half-life is approximately 2.8 hours, with a bioavailability of 20%.

At a glance

Generic nameketamine
SponsorPh Health
Drug classGeneral Anesthetic
TargetGlutamate [NMDA] receptor
Therapeutic areaMetabolic
PhaseFDA-approved
First approval1970

Mechanism of action

Ketamine Hydrochloride Injection, racemic mixture of ketamine, is non-selective, non-competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor, an ionotropic glutamate receptor. The major circulating metabolite of ketamine (norketamine) demonstrated activity at the same receptor with less affinity. Norketamine is about 1/3 as active as ketamine in reducing halothane requirements (MAC) of the rat.

Approved indications

Common side effects

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
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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