TheraRadar
Data updated: Mar 29, 2026

MVC PLUS

ASCORBIC ACID
Approved 1982-07-13
Jump to: Indications Approvals Trials Competitors Safety Patents
1
Indication
--
Phase 3 Trials
43
Years on Market

Details

Status
Discontinued
First Approved
1982-07-13
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

WATSON LABS
Active Ingredient: ASCORBIC ACID , BIOTIN , CYANOCOBALAMIN , DEXPANTHENOL , ERGOCALCIFEROL , FOLIC ACID , NIACINAMIDE , PYRIDOXINE HYDROCHLORIDE , RIBOFLAVIN 5'-PHOSPHATE SODIUM , THIAMINE HYDROCHLORIDE , VITAMIN A , VITAMIN E

MVC PLUS Approval History

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What MVC PLUS Treats

1 FDA approvals

Originally approved for its first indication in 1982 .

  • Other (1)
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

ClinicalTrials.gov ↗ Pro

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.

MVC PLUS FDA Label Details

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Data Sources

FDA Approval: NDA018439 → Patents: FDA Orange Book → Trials: ClinicalTrials.gov →

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