Friday, July 10, 2026

Drug profile · INN

isoproterenol hydrochloride

isoproterenol hydrochloride (ISOPROTERENOL HYDROCHLORIDE) is a adrenergic receptor beta agonist. Associated with Regeneron Ireland Designated Activity Company (DAC). Route of administration: rectal, sublingual. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — isoproterenol hydrochloride
US status
approved
Class
Route
RECTAL, SUBLINGUAL
Patents
0
Programs
0
Data quality
0.89

Quick answer

isoproterenol hydrochloride (ISOPROTERENOL HYDROCHLORIDE) is a adrenergic receptor beta agonist. Associated with Regeneron Ireland Designated Activity Company (DAC). Route of administration: rectal, sublingual. Current US regulatory status: approved.

Key facts

INN isoproterenol hydrochloride
Brand ISOPROTERENOL HYDROCHLORIDE
Mechanism Adrenergic receptor beta agonist
Target Adrenergic receptor beta
Route RECTAL, SUBLINGUAL
Formulation SOLUTION

Mechanism of action

Adrenergic receptor beta agonist

Primary target: Adrenergic receptor beta

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. carteolol hydrochloride Adrenergic receptor beta antagonist
  2. isoproterenol sulfate Adrenergic receptor beta agonist

Frequently asked questions

What is isoproterenol hydrochloride?

isoproterenol hydrochloride (ISOPROTERENOL HYDROCHLORIDE) is a adrenergic receptor beta agonist. Associated with Regeneron Ireland Designated Activity Company (DAC). Route of administration: rectal, sublingual. Current US regulatory status: approved.

What is the brand name for isoproterenol hydrochloride?

ISOPROTERENOL HYDROCHLORIDE is a marketed brand name for isoproterenol hydrochloride. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of isoproterenol hydrochloride?

isoproterenol hydrochloride has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.