Generic Cycloset Availability
Last updated on Sep 11, 2024.
Cycloset is a brand name of bromocriptine, approved by the FDA in the following formulation(s):
CYCLOSET (bromocriptine mesylate - tablet;oral)
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Manufacturer: VEROSCIENCE
Approval date: May 5, 2009
Strength(s): EQ 0.8MG BASE [RLD]
Has a generic version of Cycloset been approved?
No. There is currently no therapeutically equivalent version of Cycloset available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cycloset. 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: Generic Drug FAQ.
Related patents
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.
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Bromocriptine formulations
Patent 10,688,094
Issued: June 23, 2020
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓
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Combination of dopamine agonists plus first phase insulin secretagogues for the treatment of metabolic disorders
Patent 10,688,155
Issued: June 23, 2020
Inventor(s): Cincotta Anthony H.
Assignee(s): VeroScience LLCThe present invention is directed to a method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the use of an agent(s) that increases central dopaminergic activity plus a first-phase insulin secretagouge.
Patent expiration dates:
- June 7, 2030✓
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Bromocriptine formulations
Patent 11,000,522
Issued: May 11, 2021
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓
- April 30, 2032✓
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- April 30, 2032
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Bromocriptine formulations
Patent 8,431,155
Issued: April 30, 2013
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓✓
- April 30, 2032
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Bromocriptine formulations
Patent 8,613,947
Issued: December 24, 2013
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Steams Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓✓
- April 30, 2032
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Combination of dopamine agonists plus first phase secretagogues for the treatment of metabolic disorders
Patent 8,877,708
Issued: November 4, 2014
Inventor(s): Cincotta Anthony H.
Assignee(s): VeroScience, LLCThe present invention is directed to a method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the use of an agent(s) that increases central dopaminergic activity plus a first-phase insulin secretagouge.
Patent expiration dates:
- June 7, 2030✓✓
- June 7, 2030
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Bromocriptine formulations
Patent 9,192,576
Issued: November 24, 2015
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycerine control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓✓
- April 30, 2032
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Combination of dopamine agonists plus first phase insulin secretagogues for the treatment of metabolic disorders
Patent 9,352,025
Issued: May 31, 2016
Inventor(s): Cincotta Anthony H.
Assignee(s): VeroScience LLCThe present invention is directed to a method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the use of an agent(s) that increases central dopaminergic activity plus a first-phase insulin secretagouge.
Patent expiration dates:
- June 7, 2030✓
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Bromocriptine formulations
Patent 9,522,117
Issued: December 20, 2016
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓✓
- April 30, 2032✓✓
- April 30, 2032
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Bromocriptine formulations
Patent 9,700,555
Issued: July 11, 2017
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓✓
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Combination of dopamine agonists plus first phase insulin secretagogues for the treatment of metabolic disorders
Patent 9,895,422
Issued: February 20, 2018
Inventor(s): Cincotta Anthony H.
Assignee(s): VeroScience LLCThe present invention is directed to a method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the use of an agent(s) that increases central dopaminergic activity plus a first-phase insulin secretagouge.
Patent expiration dates:
- June 7, 2030✓
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Bromocriptine formulations
Patent 9,993,474
Issued: June 12, 2018
Inventor(s): Cincotta Anthony H. & Bowe Craig Michael & Stearns Paul Clark & Weston Laura Jean
Assignee(s): VeroScience LLCThe present application describes pharmaceutical formulations of bromocriptine mesylate and methods of manufacturing and using such formulations. The formulations are useful for improving glycemic control in the treatment of type 2 diabetes.
Patent expiration dates:
- April 30, 2032✓
- April 30, 2032✓
- April 30, 2032✓
- April 30, 2032✓
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More about Cycloset (bromocriptine)
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- Drug class: dopaminergic antiparkinsonism agents
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Glossary
Term | Definition |
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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. |
Further information
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