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Generic Reyvow Availability

Last updated on Nov 7, 2023.

Reyvow is a brand name of lasmiditan, approved by the FDA in the following formulation(s):

REYVOW (lasmiditan succinate - tablet;oral)

  • Manufacturer: ELI LILLY AND CO
    Approval date: January 31, 2020
    Strength(s): EQ 50MG BASE [RLD], EQ 100MG BASE [RLD]
  • Manufacturer: ELI LILLY AND CO
    Approval date: December 18, 2020
    Strength(s): EQ 200MG BASE (discontinued) [RLD]

Has a generic version of Reyvow been approved?

No. There is currently no therapeutically equivalent version of Reyvow available in the United States.

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Reyvow. 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.

  • Compositions and methods related to pyridinoylpiperidine 5-HTagonists
    Patent 11,053,214
    Issued: July 6, 2021
    Inventor(s): Allieri Brigida & Fagan Paul & Sharp Emma & Skwierczynski Raymond D.
    Assignee(s): CoLucid Pharmaceuticals, Inc.

    The present invention provides new pseudo-polymorphs of the hemisuccinate salt of 2,4,6-trifluoro-N-[6-(1-methyl-piperidine-4-carbonyl)-pyridin-2-yl]-benzamide which are useful in pharmaceutical compositions, for example, for the treatment and prevention of migraine headache.

    Patent expiration dates:

    • December 5, 2037
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE
      ✓ 
      Drug substance
      ✓ 
      Drug product
  • Patent 7,423,050
    Issued: November 30, -0001

    Patent expiration dates:

    • February 17, 2028
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE
      ✓ 
      Drug substance
      ✓ 
      Drug product
  • Pyridinoylpiperidines as 5-HTagonists
    Patent 8,748,459
    Issued: June 10, 2014
    Inventor(s): Cohen Michael Philip & Kohlman Daniel Timothy & Liang Sidney Xi & Victor Frantz & Xu Yao-Chang & Ying Bai-Ping & Zacherl DeAnna Piatt & Zhang Deyi
    Assignee(s): Eli Lilly and Company

    The present invention relates to compounds of formula I:

    Patent expiration dates:

    • March 27, 2023
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE

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 31, 2025 - NEW CHEMICAL ENTITY

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.

Medical Disclaimer