Generic VESIcare Availability
VESICARE (solifenacin succinate - tablet;oral)
Has a generic version of VESIcare been approved?
No. There is currently no therapeutically equivalent version of VESIcare available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of VESIcare. 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.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Quinuclidine derivatives and medicinal composition thereof
Issued: January 25, 2000
Inventor(s): Takeuchi; Makoto & Naito; Ryo & Hayakawa; Masahiko & Okamoto; Yoshinori & Yonetoku; Yasuhiro & Ikeda; Ken & Isomura; Yasuo
Assignee(s): Yamanouchi Pharmaceutical Co., Ltd.
Quinuclidine derivatives represented by general following general formula (I), salts, N-oxides or quaternary ammonium salts thereof, and medicinal compositions containing the same. ##STR1## The compound has an antagonistic effect on muscarinic M.sub.3 receptors and is useful as a preventive or remedy for urologic diseases, respiratory diseases or digestive diseases.Patent expiration dates:
- November 19, 2018✓✓
- November 19, 2018
- Vesicare Consumer Information (Drugs.com)
- VESIcare Consumer Information (Wolters Kluwer)
- VESIcare Consumer Information (Cerner Multum)
- Vesicare Advanced Consumer Information (Micromedex)
- Vesicare AHFS DI Monographs (ASHP)
- Solifenacin Consumer Information (Wolters Kluwer)
- Solifenacin Consumer Information (Cerner Multum)
- Solifenacin Advanced Consumer Information (Micromedex)
- Solifenacin Succinate AHFS DI Monographs (ASHP)
|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.|