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Data updated: Mar 10, 2026

LODOSYN

CARBIDOPA DOPA Decarboxylase Inhibitors
Neurology Approved 1977-04-25
1
Indication
--
Phase 3 Trials
1
Priority Reviews
48
Years on Market

Details

Status
Prescription
First Approved
1977-04-25
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: CARBIDOPA

LODOSYN Approval History

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What LODOSYN Treats

2 indications

LODOSYN is approved for 2 conditions since its original approval in 1977. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Parkinson's Disease
  • Parkinsonism
Source: FDA Label

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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.

LODOSYN FDA Label Details

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Indications & Usage

FDA Label (PDF)

LODOSYN is indicated for use with carbidopa-levodopa or with levodopa in the treatment of the symptoms of idiopathic Parkinson’s disease (paralysis agitans), postencephalitic parkinsonism, and symptomatic parkinsonism, which may follow injury to the nervous system by carbon monoxide intoxication and/or manganese intoxication. LODOSYN is for use with carbidopa-levodopa in patients for whom the dosage of carbidopa-levodopa provides less than adequate daily dosage (usually 70 mg daily) of carbidopa. LODOSYN is for use with levodopa in the occasional patient whose dosage requirement of carbidopa a...

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Data Sources

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