ENTERO VU 24%
Details
- Status
- Prescription
- First Approved
- 2016-01-15
- Routes
- ORAL
- Dosage Forms
- SUSPENSION
ENTERO VU 24% Approval History
What ENTERO VU 24% Treats
7 FDA approvalsOriginally approved for its first indication in 2016 . Covers 7 distinct patient populations.
- Other (7)
Other
(7 approvals)- • Approved indication (Jan 2016)Label Letter
- • Approved indication (Mar 2017)Label Letter
- • Approved indication (Jul 2017)Label Letter
- • Approved indication (Aug 2017)Label Letter
- • Approved indication (Jan 2018)Label Letter
- • Approved indication (Mar 2018)Label Letter
- • Approved indication (May 2020)Label Letter
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
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.
ENTERO VU 24% FDA Label Details
ProIndications & Usage
FDA Label (PDF)ENTERO VU 24% is indicated for use in small bowel radiographic examinations to visualize the gastrointestinal (GI) tract in adult patients. ENTERO VU 24% is a radiographic contrast agent indicated for use in small bowel radiographic examinations to visualize the gastrointestinal (GI) tract in adult patients
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.