Friday, July 10, 2026

Drug profile · INN

beclomethasone dipropionate monohydrate

beclomethasone dipropionate monohydrate (VANCENASE AQ) is a glucocorticoid receptor agonist. Route of administration: nasal. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — beclomethasone dipropionate monohydrate
US status
approved
Class
Route
NASAL
Patents
0
Programs
0
Data quality
0.84

Quick answer

beclomethasone dipropionate monohydrate (VANCENASE AQ) is a glucocorticoid receptor agonist. Route of administration: nasal. Current US regulatory status: approved.

Key facts

INN beclomethasone dipropionate monohydrate
Brand VANCENASE AQ
Mechanism Glucocorticoid receptor agonist
Target Glucocorticoid receptor
Route NASAL
Formulation SPRAY, METERED

Mechanism of action

Glucocorticoid receptor agonist

Primary target: Glucocorticoid receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. beclomethasone dipropionate Glucocorticoid receptor agonist
  2. betamethasone acetate Glucocorticoid receptor agonist
  3. betamethasone dipropionate Glucocorticoid receptor agonist
  4. betamethasone valerate Glucocorticoid receptor agonist
  5. budesonide Alimentary tract and metabolism (A07)
  6. clobetasol propionate Glucocorticoid receptor agonist

Frequently asked questions

What is beclomethasone dipropionate monohydrate?

beclomethasone dipropionate monohydrate (VANCENASE AQ) is a glucocorticoid receptor agonist. Route of administration: nasal. Current US regulatory status: approved.

What is the brand name for beclomethasone dipropionate monohydrate?

VANCENASE AQ is a marketed brand name for beclomethasone dipropionate monohydrate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of beclomethasone dipropionate monohydrate?

beclomethasone dipropionate monohydrate 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.