NDAINTRAVENOUSSOLUTION
Approved
Oct 2025
Lifecycle
Launch
Competitive Pressure
0/100
Clinical Trials
2
Data completeness
4/8 — Partial
ROCURONIUM BROMIDE (rocuronium bromide) by B. Braun is duration. First approved in 2025.
Drug data last refreshed 10h ago · AI intelligence enriched 5d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Rocuronium bromide is a neuromuscular blocking agent administered intravenously as a solution. It works by competing for cholinergic receptors at the motor end-plate, with effects antagonized by acetylcholinesterase inhibitors such as neostigmine and edrophonium. Used in anesthesia and critical care settings to facilitate intubation and muscle relaxation during surgical procedures.
Launch12.8 years to LOE
Early-stage launch with no current competitive pressure; commercial team building and market establishment phase represent growth opportunity for field and marketing roles.
Mechanism of Action
duration. It acts by competing for cholinergic receptors at the motor end-plate. This action is antagonized by acetylcholinesterase inhibitors, such as neostigmine and edrophonium.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (2)
A Study to Determine the Dose Requirements of Rocuronium Bromide (Zemuron®) in Pediatric and Adolescent Subjects (21048)(COMPLETED)(P05797)
Started Oct 2004
149 enrolled
Anesthesia
Dose-Finding Trial With Sugammadex Administered at 3 and 15 Minutes After 1.0 and 1.2 mg/kg Rocuronium Bromide in Participants of ASA Class 1-3 (P05944; MK-8616-024)
Started Mar 2004
174 enrolled
Anesthesia, General
Career Relevance
Rocuronium bromide represents a launch-stage opportunity in the stable anesthesia market, with immediate needs in commercial execution, healthcare provider education, and supply chain establishment. Career professionals joining now will build the brand infrastructure during its critical first years with competitive advantages from established patent protection and sponsor manufacturing capabilities.
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.