Generic Jesduvroq Availability
Last updated on Jun 11, 2025.
Jesduvroq is a brand name of daprodustat, approved by the FDA in the following formulation(s):
JESDUVROQ (daprodustat - tablet;oral)
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Manufacturer: GLAXOSMITHKLINE
Approval date: February 1, 2023
Strength(s): 1MG (discontinued) [RLD], 2MG (discontinued) [RLD], 4MG (discontinued) [RLD], 6MG (discontinued) [RLD], 8MG (discontinued) [RLD]
All of the above formulations have been discontinued.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Jesduvroq. 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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Crystalline forms of GSK1278863, preparation method and pharmaceutical use thereof
Patent 11,117,871
Issued: September 14, 2021
Inventor(s): Chen; Minhua et al.
Assignee(s): GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (Brentford, GB)The present disclosure relates to crystalline form CS1 and CS9 of a hypoxia-inducible factor prolyl hydroxylase inhibitor compound (I) GSK1278863, processes for preparation, and uses for preparing drugs treating and/or preventing anemia thereof. ##STR00001##
Patent expiration dates:
- March 13, 2038✓✓✓
- March 13, 2038
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Prolyl hydroxylase inhibitors
Patent 11,643,397
Issued: May 9, 2023
Inventor(s): Duffy; Kevin J. et al.
Assignee(s): GlaxoSmithKline LLC (Wilmington, DE)The invention described herein relates to certain pyrimidinetrione N-substituted glycine derivatives of formula (I) ##STR00001##
which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.Patent expiration dates:
- June 22, 2027✓✓
- June 22, 2027
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Crystalline forms of GSK1278863, preparation method and pharmaceutical use thereof
Patent 11,649,217
Issued: May 16, 2023
Inventor(s): Chen; Minhua et al.
Assignee(s): GlaxoSmithKline Intellectual Property (NO.2) Limited (Brentford, GB)The present disclosure relates to crystalline form CS1 and CS9 of a hypoxia-inducible factor prolyl hydroxylase inhibitor compound (I) GSK1278863, processes for preparation, and uses for preparing drugs treating and/or preventing anemia thereof. ##STR00001##
Patent expiration dates:
- March 13, 2038✓✓
- March 13, 2038
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Prolyl hydroxylase inhibitors
Patent 8,324,208
Issued: December 4, 2012
Inventor(s): Duffy Kevin J. & Fitch Duke M. & Jin Jian & Liu Ronggang & Shaw Antony N. & Wiggall Kenneth
Assignee(s): GlaxoSmithKline LLCThe invention described herein relates to certain pyrimidinetrione N-substituted glycine derivatives of formula (I)
Patent expiration dates:
- December 11, 2028✓✓
- December 11, 2028
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Prolyl hydroxylase inhibitors
Patent 8,557,834
Issued: October 15, 2013
Inventor(s): Fitch Duke M. & Shaw Antony N. & Wiggall Kenneth
Assignee(s): GlaxoSmithKline LLCThe invention described herein relates to certain pyrimidinetrione N-substituted glycine derivatives of formula (I)
Patent expiration dates:
- June 22, 2027✓
- June 22, 2027
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Prolyl hydroxylase inhibitors
Patent 8,815,884
Issued: August 26, 2014
Inventor(s): Fitch Duke M. & Shaw Antony N. & Wiggall Kenneth
Assignee(s): GlaxoSmithKline LLCThe invention described herein relates to certain pyrimidinetrione N-substituted glycine derivatives of formula (I)
Patent expiration dates:
- June 22, 2027✓✓
- June 22, 2027
Related exclusivities
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
Exclusivity expiration dates:
- February 1, 2028 - NEW CHEMICAL ENTITY
More about Jesduvroq (daprodustat)
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- Drug class: miscellaneous uncategorized agents
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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. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.