TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

QUIOFIC

FOLIC ACID
Hematology Approved 2026-01-26
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2026-01-26
Routes
ORAL
Dosage Forms
SOLUTION

Companies

Active Ingredient: FOLIC ACID

QUIOFIC Approval History

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What QUIOFIC Treats

2 indications

QUIOFIC is approved for 2 conditions since its original approval in 2026. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Megaloblastic Anemia
  • Folic Acid Deficiency
Source: FDA Label

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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.

QUIOFIC FDA Label Details

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Indications & Usage

QUIOFIC is indicated for the treatment of megaloblastic anemias due to folic acid deficiency in adult and pediatric patients. QUIOFIC is a folate analog indicated for the treatment of megaloblastic anemias due to folic acid deficiency in adult and pediatric patients.

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Data Sources

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