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Generic Lyrica Availability

See also: Generic Lyrica CR

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

LYRICA (pregabalin - capsule;oral)

  • Manufacturer: PF PRISM CV
    Approval date: December 30, 2004
    Strength(s): 25MG [RLD], 50MG [RLD], 75MG [RLD], 100MG [RLD], 150MG [RLD], 200MG [RLD], 225MG [RLD], 300MG [RLD]

LYRICA (pregabalin - solution;oral)

  • Manufacturer: PF PRISM CV
    Approval date: January 4, 2010
    Strength(s): 20MG/ML [RLD]

Has a generic version of Lyrica been approved?

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

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

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.

  • Isobutylgaba and its derivatives for the treatment of pain
    Patent 6,001,876
    Issued: December 14, 1999
    Inventor(s): Singh; Lakhbir
    Assignee(s): Warner-Lambert Company

    The instant invention is a method of using certain analogs of glutamic acid and gamma-aminobutyric acid in pain therapy.

    Patent expiration dates:

    • June 30, 2019
      ✓ 
      Pediatric exclusivity
  • Gamma amino butyric acid analogs and optical isomers
    Patent 6,197,819
    Issued: March 6, 2001
    Inventor(s): Silverman; Richard B. & Andruszkiewicz; Ryszard
    Assignee(s): Northwestern University

    A compound of the formula ##STR1## wherein R.sub.1 is a straight or branched alkyl group having from 1 to 6 carbon atoms, phenyl, or cycloalkyl having from 3 to 6 carbon atoms; R.sub.2 is hydrogen or methyl; and R.sub.3 is hydrogen, methyl or carboxyl; which is useful in the treatment of seizure disorders. Processes are disclosed for the preparation of the compound. Intermediates prepared during the synthesis of the compound are also disclosed.

    Patent expiration dates:

    • June 30, 2019
      ✓ 
      Pediatric exclusivity
  • Isobutylgaba and its derivatives for the treatment of pain
    Patent RE41920
    Issued: November 9, 2010
    Inventor(s): Singh; Lakhbir
    Assignee(s): Warner-Lambert Company LLC

    The instant invention is a method of using certain analogs of glutamic acid and gamma-aminobutyric acid in pain therapy.

    Patent expiration dates:

    • June 30, 2019
      ✓ 
      Pediatric exclusivity

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:

    • December 22, 2019 - INFORMATION ADDED TO THE LABELING REGARDING A 15-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, PLACEBO-CONTROLLED FLEXIBLE-DOSE SAFETY AND EFFICACY STUDY OF PREGABALIN IN ADOLESCENTS (12 THROUGH 17 YEARS OLD) WITH FIBROMYALGIA
    • June 22, 2020 - PEDIATRIC EXCLUSIVITY
    • May 3, 2021 - NEW PATIENT POPULATION
    • November 3, 2021 - PEDIATRIC EXCLUSIVITY

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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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.

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