Data updated: Mar 10, 2026
GO-EVAC
POLYETHYLENE GLYCOL 3350
Approved 1992-04-28
1
Indication
--
Phase 3 Trials
33
Years on Market
Details
- Status
- Discontinued
- First Approved
- 1992-04-28
- Routes
- ORAL
- Dosage Forms
- FOR SUSPENSION
Companies
Active Ingredient: POLYETHYLENE GLYCOL 3350 , POTASSIUM CHLORIDE , SODIUM BICARBONATE , SODIUM CHLORIDE , SODIUM SULFATE ANHYDROUS
Website: โ
GO-EVAC Approval History
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What GO-EVAC Treats
1 FDA approvalsOriginally approved for its first indication in 1992 .
- Other (1)
Other
(1 approval)- โข Approved indication (Apr 1992)
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Pro Active Pipeline
Ongoing clinical trials by development phase
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โญ
Pro Key Completed Trials
Completed studies with published results, ranked by significance
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๐
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.
GO-EVAC FDA Label Details
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.