There are no generic versions of Flovent HFA or Flovent Diskus licensed for sale at this time. The earliest date that a generic version of Flovent HFA could become available is December 2012; the earliest that a generic Flovent Diskus could become available is February 2016. However, certain circumstances (such as lawsuits) could come up to extend the exclusivity periods of these medications.
"HFA" stands for hydrofluoroalkane, which is the propellant used in Flovent HFA inhalers. Because this inhaler uses hydrofluoroalkane, it is environmentally friendly. This has replaced the old Flovent® inhaler, which contained substances that may deplete the ozone layer. The Flovent Diskus is a dry powder inhaler device.
Flovent is manufactured by GlaxoSmithKline. It is currently under the protection of patents that prevent any generic Flovent from being manufactured in the United States.
When Will Generic Flovent Be Available?
The first patent for Flovent HFA currently expires in December 2012; the first patent for Flovent Diskus expired in September 2011, although no generic versions are available. This suggests that later-expiring patents are still protecting the Flovent Diskus from generic competition. The next Flovent Diskus patent will expire in February 2016.
At this point, these are the earliest possible dates that a generic version of Flovent HFA or Flovent Diskus could become available. However, there are circumstances that could come up to extend the exclusivity period of Flovent. These circumstances could include things such as other patents for specific Flovent uses or lawsuits. Once Flovent goes off patent, there may be several companies that manufacture a generic Flovent product.
Written by/reviewed by: Kristi Monson, PharmD;Arthur Schoenstadt, MD
Last reviewed by: KristiMonson, PharmD;
List of references (click here):
Flovent HFA [package insert]. Research Triangle Park, NC: GlaxoSmithKline;2007 January.
Flovent Diskus [package insert]. Research Triangle Park, NC: GlaxoSmithKline;2006 November.
Food and Drug Administration, Center for Drug Evaluation and Research. Electronic orange book: approved drug products with therapeutic equivalence evaluations. FDA Web site. Available at: http://www.fda.gov/cder/ob/. Accessed February 9, 2012.
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