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Generic Suprax Availability

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

SUPRAX (cefixime - capsule;oral)

  • Manufacturer: LUPIN LTD
    Approval date: June 1, 2012
    Strength(s): 400MG [RLD]

SUPRAX (cefixime - for suspension;oral)

  • Manufacturer: LEDERLE
    Approval date: April 28, 1989
    Strength(s): 100MG/5ML
  • Manufacturer: LUPIN LTD
    Approval date: February 20, 2013
    Strength(s): 500MG/5ML [RLD]

SUPRAX (cefixime - tablet;oral)

  • Manufacturer: LEDERLE
    Approval date: April 28, 1989
    Strength(s): 200MG, 400MG

Has a generic version of Suprax been approved?

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

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Suprax. 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: About generic drugs.

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.

  • Pharmaceutical compositions of cefixime
    Patent 9,233,112
    Issued: January 12, 2016
    Assignee(s): LUPIN LIMITED
    A pharmaceutical suspension dosage form comprising greater than 80 mg/ml and not more than 150 mg/ml of Cefixime and pharmaceutically acceptable excipients.
    Patent expiration dates:
    • December 14, 2028
      Drug product


Drug PatentA 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 ExclusivityExclusivity 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.
RLDA 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.