Data updated: Mar 10, 2026
MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 7.4
MAGNESIUM CHLORIDE
Approved 2022-06-08
1
Indication
--
Phase 3 Trials
3
Years on Market
Details
- Status
- Prescription
- First Approved
- 2022-06-08
- Routes
- INJECTION
- Dosage Forms
- INJECTABLE
Companies
Active Ingredient: MAGNESIUM CHLORIDE , POTASSIUM CHLORIDE , SODIUM ACETATE , SODIUM CHLORIDE , SODIUM GLUCONATE
Website: ↗
MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 7.4 Approval History
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What MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 7.4 Treats
1 FDA approvalsOriginally approved for its first indication in 2022 .
- Other (1)
Other
(1 approval)- • Approved indication (Jun 2022)Letter
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Pro Active Pipeline
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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.
MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 7.4 FDA Label Details
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.