NDAINTRAVENOUSSOLUTION
Approved
Apr 2023
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
6
Data completeness
5/8 — Partial
ADRENALIN (epinephrine in sodium chloride) by Pfizer is adrenergic alpha-agonists [moa]. First approved in 2023.
Drug data last refreshed 1h ago · AI intelligence enriched 1h ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ADRENALIN is an intravenous solution containing epinephrine in sodium chloride, approved by the FDA in April 2023. It is an alpha-adrenergic agonist indicated for acute hemodynamic support in critical care settings. The drug works by stimulating alpha-adrenergic receptors to increase vascular resistance and blood pressure.
$0.051BPart D
Peak12.5 years to LOEEarly-stage peak sales trajectory with modest Part D utilization indicates focused hospital/critical care positioning rather than broad retail penetration.
Mechanism of Action
Adrenergic alpha-Agonists
Pharmacologic Class:
alpha-Adrenergic Agonist
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (6)
Study Evaluating the Safety and Efficacy of Neffy or Intramuscular Adrenalin in Patients With Allergic Reactions After Oral Food Challenge or Allergen Immunotherapy
Started May 2025
600 enrolled
Allergic Reactions
Comparative Efficacy of Hypertonic Saline vs Adrenaline Nebulization in Acute Bronchiolitis
Started Nov 2023
60 enrolled
Acute Bronchiolitis Due to Respiratory Syncytial Virus
Pharmacokinetics of Adrenaline After Administration of ARS -1 in Subjects With Upper Respiratory Tract Infection
Started Aug 2021
15 enrolled
Upper Respiratory Tract Infection
Changes in Striatal [11C]ORM-13070 Binding Elicited by Changing Levels of Endogenous Noradrenaline
Started Aug 2012
8 enrolled
Changes in Striatal [11C]ORM-13070 Binding.
Comparative Evaluation of Handling Characteristics of Two Adrenaline Autoinjectors,EpiPen in Comparison With Jext
Started Jan 2012
91 enrolled
Handling of Auto-injectors
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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.