Generic Cardura XL Availability
See also: Generic Cardura
Cardura XL is a brand name of doxazosin, approved by the FDA in the following formulation(s):
CARDURA XL (doxazosin mesylate - tablet, extended release; oral)
Has a generic version of Cardura XL been approved?
No. There is currently no therapeutically equivalent version of Cardura XL available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cardura XL. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Related Patents
There are no current U.S. patents associated with Cardura XL.
See also...
- Cardura XL extended-release tablets Consumer Information (Wolters Kluwer)
- Cardura XL Consumer Information (Cerner Multum)
- Cardura XL Advanced Consumer Information (Micromedex)
- Doxazosin Consumer Information (Drugs.com)
- Doxazosin Consumer Information (Wolters Kluwer)
- Doxazosin extended-release tablets Consumer Information (Wolters Kluwer)
- Doxazosin Consumer Information (Cerner Multum)
- Doxazosin Advanced Consumer Information (Micromedex)
- Doxazosin Mesylate AHFS DI Monographs (ASHP)
Glossary
| Term | Definition |
|---|---|
| Drug Patent | A drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation. |
| Drug Exclusivity | Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant. |
| RLD | A Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. |
