TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

KETALAR

KETAMINE HYDROCHLORIDE
Approved 1970-02-19
2
Indications
--
Phase 3 Trials
1
Priority Reviews
56
Years on Market

Details

Status
Prescription
First Approved
1970-02-19
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: KETAMINE HYDROCHLORIDE

KETALAR Approval History

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What KETALAR Treats

2 FDA approvals

Originally approved for its first indication in 1970 . Covers 2 distinct patient populations.

  • Other (2)
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

KETALAR FDA Label Details

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Indications & Usage

FDA Label (PDF)

KETALAR (ketamine hydrochloride) injection is indicated: as the sole anesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. for the induction of anesthesia prior to the administration of other general anesthetic agents. as a supplement to other anesthetic agents. KETALAR is a general anesthetic indicated: as the sole anesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation for the induction of anesthesia prior to the administration of other general anesthetic agents as a supplement to other anestheti...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.