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Ketamine Injectable Product

Hackensack Meridian Health · FDA-approved active Small molecule ✓ Verified May 2026

Ketamine Injectable Product is a NMDA receptor antagonist Small molecule drug developed by Hackensack Meridian Health. It is currently FDA-approved for Induction and maintenance of anesthesia, Analgesia and sedation, Treatment-resistant depression (off-label/emerging indication). Also known as: Ketalar, Ketalar Hydrocholoride.

Ketamine is a non-competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor that blocks glutamate signaling in the central nervous system.

Ketamine is a small molecule medication used to treat various conditions, including asthma exacerbations, pain, and analgesia. It is administered through nebulization, typically at a dose of 0.5 mg/kg in normal saline, or through other methods such as ultrasound-guided facia iliaca block.

At a glance

Generic nameKetamine Injectable Product
Also known asKetalar, Ketalar Hydrocholoride
SponsorHackensack Meridian Health
Drug classNMDA receptor antagonist
TargetNMDA receptor
ModalitySmall molecule
Therapeutic areaAnesthesia, Pain Management, Psychiatry
PhaseFDA-approved

Mechanism of action

Ketamine binds to the phencyclidine binding site within the NMDA receptor ion channel, blocking the flow of ions and preventing excitatory neurotransmission. This mechanism produces rapid-onset anesthetic and analgesic effects, and at sub-anesthetic doses, it has been shown to produce rapid antidepressant effects through modulation of glutamatergic and other neurotransmitter systems.

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
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Ketamine Injectable Product

What is Ketamine Injectable Product?

Ketamine Injectable Product is a NMDA receptor antagonist drug developed by Hackensack Meridian Health, indicated for Induction and maintenance of anesthesia, Analgesia and sedation, Treatment-resistant depression (off-label/emerging indication).

How does Ketamine Injectable Product work?

Ketamine is a non-competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor that blocks glutamate signaling in the central nervous system.

What is Ketamine Injectable Product used for?

Ketamine Injectable Product is indicated for Induction and maintenance of anesthesia, Analgesia and sedation, Treatment-resistant depression (off-label/emerging indication).

Who makes Ketamine Injectable Product?

Ketamine Injectable Product is developed and marketed by Hackensack Meridian Health (see full Hackensack Meridian Health pipeline at /company/hackensack-meridian-health).

Is Ketamine Injectable Product also known as anything else?

Ketamine Injectable Product is also known as Ketalar, Ketalar Hydrocholoride.

What drug class is Ketamine Injectable Product in?

Ketamine Injectable Product belongs to the NMDA receptor antagonist class. See all NMDA receptor antagonist drugs at /class/nmda-receptor-antagonist.

What development phase is Ketamine Injectable Product in?

Ketamine Injectable Product is FDA-approved (marketed).

What are the side effects of Ketamine Injectable Product?

Common side effects of Ketamine Injectable Product include Dissociation, Dizziness, Nausea, Increased blood pressure, Hallucinations, Emergence reactions.

What does Ketamine Injectable Product target?

Ketamine Injectable Product targets NMDA receptor and is a NMDA receptor antagonist.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing