Sold as Beconase Aq, Vancenase Aq. Every FDA application for this active ingredient.
As of Nov 15, 2026, FDA lists 3 applications for Beclomethasone Dipropionate Monohydrate (sold as Beconase Aq, Vancenase Aq), first approved Jul 27, 1987, with 0 new uses approved and 0 published complete response letters.
| Jul 27, 1987 | Beconase AqNDA 19389 · New dosage form | Glaxosmithkline | 22 | Discontinued |
| Dec 23, 1987 | Vancenase AqNDA 19589 · New formulation or manufacturer | Schering | 5 | Discontinued |
| Jun 26, 1996 | Vancenase AqNDA 20469 · New dosage form | Schering | 6 | Discontinued |
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient. Drugs@FDA