TheraRadar
Data updated: Nov 8, 2026

VYDUO (nebivolol hydrochloride) · PRINSTON INC

Cardiovascular Approved 2022-09-19
FDA label not available. This product's label is not in FDA's label database (openFDA, DailyMed). Search DailyMed → · Drugs@FDA approval documents →
1
Indication
--
Phase 3 Trials
4
Years on Market

Details

Status
Prescription
First Approved
2022-09-19
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: NEBIVOLOL HYDROCHLORIDE , VALSARTAN

VYDUO Approval History

2023
2024
2025
2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2022 to 2022
Sep 2022 ORIGINAL
Update

What VYDUO Treats

1 FDA approvals

Originally approved for its first indication in 2022 .

  • Other (1)
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Active Pipeline

Pro

Ongoing clinical trials by development phase

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Key Completed Trials

Pro

Completed studies with published results, ranked by significance

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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.

VYDUO FDA Label Details

FDA label not available. This product's label is not in FDA's label database (openFDA, DailyMed). Search DailyMed → · Drugs@FDA approval documents →

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Data Sources

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