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Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

MANGANESE CHLORIDE IN PLASTIC CONTAINER

MANGANESE CHLORIDE
Approved 1986-06-26
1
Indication
--
Phase 3 Trials
1
Priority Reviews
39
Years on Market

Details

Status
Prescription
First Approved
1986-06-26
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: MANGANESE CHLORIDE

MANGANESE CHLORIDE IN PLASTIC CONTAINER Approval History

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What MANGANESE CHLORIDE IN PLASTIC CONTAINER Treats

1 indications

MANGANESE CHLORIDE IN PLASTIC CONTAINER is approved for 1 conditions since its original approval in 1986. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Manganese Deficiency
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.

MANGANESE CHLORIDE IN PLASTIC CONTAINER FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

Manganese 0.1 mg/mL (Manganese Chloride Injection, USP) is indicated for use in adult patients as a supplement to intravenous solutions given for TPN. Administration helps to maintain manganese serum levels and to prevent depletion of endogenous stores and subsequent deficiency symptoms.

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Data Sources

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