Generic Journavx Availability
Last updated on Apr 10, 2025.
Journavx is a brand name of suzetrigine, approved by the FDA in the following formulation(s):
JOURNAVX (suzetrigine - tablet;oral)
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Manufacturer: VERTEX PHARMS INC
Approval date: January 30, 2025
Strength(s): 50MG [RLD]
Is there a generic version of Journavx available?
No. There is currently no therapeutically equivalent version of Journavx available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Journavx. 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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Substituted tetrahydrofurans as modulators of sodium channels
Patent 11,834,441
Issued: December 5, 2023
Inventor(s): Durrant; Steven John et al.
Assignee(s): VERTEX PHARMACEUTICALS INCORPORATED (Boston, MA)Compounds, and pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels are provided. Also provided are pharmaceutical compositions comprising the compounds or pharmaceutically acceptable salts and methods of using the compounds, pharmaceutically acceptable salts, and pharmaceutical compositions in the treatment of various disorders, including pain.
Patent expiration dates:
- December 4, 2040✓✓✓
- December 4, 2040
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:
- January 30, 2030 - NEW CHEMICAL ENTITY
More about Journavx (suzetrigine)
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- Drug class: miscellaneous analgesics
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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.
