TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

NESACAINE-MPF

CHLOROPROCAINE HYDROCHLORIDE
Approved 1955-03-11
1
Indication
--
Phase 3 Trials
1
Priority Reviews
71
Years on Market

Details

Status
Prescription
First Approved
1955-03-11
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: CHLOROPROCAINE HYDROCHLORIDE

NESACAINE-MPF Approval History

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What NESACAINE-MPF Treats

1 indications

NESACAINE-MPF is approved for 1 conditions since its original approval in 1955. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Local Anesthesia
Source: FDA Label
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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.

NESACAINE-MPF FDA Label Details

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Indications & Usage

FDA Label (PDF)

Chloroprocaine hydrochloride injection 2% and 3%, in single dose vials, without methylparaben preservative, without EDTA, is indicated for the production of local anesthesia by infiltration, peripheral and central nerve block, including lumbar and caudal epidural blocks. Chloroprocaine hydrochloride injection is not to be used for subarachnoid administration.

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Data Sources

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