Generic Lescol XL Availability
See also: Generic Lescol
LESCOL XL (fluvastatin sodium - tablet, extended release;oral)
Approval date: October 6, 2000
Strength(s): 80MG [RLD]
Has a generic version of Lescol XL been approved?
No. There is currently no therapeutically equivalent version of Lescol XL available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Lescol 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.
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.
Issued: June 5, 2001
Inventor(s): Kalb; Oskar Michael & Valazza; Stephen John
Assignee(s): Novartis AG
An oral dosage form comprising fluvastatin and HPMC, which oral dosage form is color-stable upon prolonged periods of storage.Patent expiration dates:
- April 13, 2020
- October 13, 2020✓
- April 13, 2020
- Lescol XL extended-release tablets Consumer Information (Wolters Kluwer)
- Lescol XL Consumer Information (Cerner Multum)
- Lescol XL Advanced Consumer Information (Micromedex®)
- Fluvastatin Consumer Information (Wolters Kluwer)
- Fluvastatin extended-release tablets Consumer Information (Wolters Kluwer)
- Fluvastatin Consumer Information (Cerner Multum)
- Fluvastatin Advanced Consumer Information (Micromedex®)
- Fluvastatin Sodium 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.|