TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

BYFAVO

REMIMAZOLAM BESYLATE
Approved 2020-07-02
1
Indication
--
Phase 3 Trials
5
Years on Market

Details

Status
Prescription
First Approved
2020-07-02
Routes
INTRAVENOUS
Dosage Forms
POWDER

Companies

Active Ingredient: REMIMAZOLAM BESYLATE

BYFAVO Approval History

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What BYFAVO Treats

1 indications

BYFAVO is approved for 1 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Procedural Sedation
Source: FDA Label

BYFAVO Boxed Warning

PERSONNEL AND EQUIPMENT FOR MONITORING AND RESUSCITATION AND RISKS FROM CONCOMITANT USE WITH OPIOID ANALGESICS WARNING: PERSONNEL AND EQUIPMENT FOR MONITORING AND RESUSCITATION, AND RISKS FROM CONCOMITANT USE WITH OPIOID ANALGESICS AND OTHER SEDATIVE-HYPNOTICS See full prescribing information for complete boxed warning Only personnel trained in the administration of procedural sedation, and not involved in the conduct of the diagnostic or therapeutic procedure, should administer BYFAVO. ( 2.1 , ...

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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

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.

BYFAVO FDA Label Details

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Indications & Usage

FDA Label (PDF)

BYFAVO ® is indicated for the induction and maintenance of procedural sedation in adults undergoing procedures lasting 30 minutes or less. BYFAVO (remimazolam) for injection is a benzodiazepine indicated for the induction and maintenance of procedural sedation in adults undergoing procedures lasting 30 minutes or less.

⚠️ BOXED WARNING

WARNING: PERSONNEL AND EQUIPMENT FOR MONITORING AND RESUSCITATION AND RISKS FROM CONCOMITANT USE WITH OPIOID ANALGESICS WARNING: PERSONNEL AND EQUIPMENT FOR MONITORING AND RESUSCITATION, AND RISKS FROM CONCOMITANT USE WITH OPIOID ANALGESICS AND OTHER SEDATIVE-HYPNOTICS See full prescribing informati...

BYFAVO Patents & Exclusivity

Latest Patent: Jan 2034

Patents (11 active)

US9827251 Expires Jan 13, 2034
US9561236 Expires Apr 30, 2033
US9737547 Expires Nov 7, 2031
US10052334 Expires Nov 7, 2031
US10195210 Expires Nov 7, 2031
US10342800 Expires Nov 7, 2031
US10722522 Expires Nov 7, 2031
US10961250 Expires Jul 10, 2027
US10472365 Expires Jul 10, 2027
US9777007 Expires Jul 10, 2027
+ 1 more patents
Source: FDA Orange Book

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Data Sources

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