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Generic Emend Availability

Last updated on Aug 10, 2022.

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

EMEND (aprepitant - capsule;oral)

  • Manufacturer: MERCK
    Approval date: March 26, 2003
    Strength(s): 80MG [RLD] [AB], 125MG [RLD] [AB]
  • Manufacturer: MERCK
    Approval date: June 30, 2006
    Strength(s): 40MG (discontinued) [RLD]

EMEND (aprepitant - for suspension;oral)

  • Manufacturer: MSD MERCK CO
    Approval date: December 17, 2015
    Strength(s): 125MG/KIT [RLD]

Has a generic version of Emend been approved?

A generic version of Emend has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Emend and have been approved by the FDA:

aprepitant capsule;oral

  • Manufacturer: GLENMARK PHARMS SA
    Approval date: October 12, 2017
    Strength(s): 80MG [AB], 125MG [AB]
  • Manufacturer: SANDOZ
    Approval date: September 24, 2012
    Strength(s): 80MG [AB], 125MG [AB]
  • Manufacturer: TORRENT
    Approval date: October 21, 2020
    Strength(s): 80MG [AB], 125MG [AB]

Note: No generic formulation of the following product is available.

  • aprepitant - for suspension;oral

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

  • Pharmaceutical composition of a tachykinin receptor antagonist
    Patent 8,258,132
    Issued: September 4, 2012
    Inventor(s): Bosch; H. William & Liversidge; Elaine & Shelukar; Suhas D. & Thompson; Karen C.
    Assignee(s): Merck Sharp & Dohme Corp.

    The present invention is directed to novel pharmaceutical compositions of the compound 2-(R)-(1-(R)-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-3-(S)-(4-fluoro)phenyl-4-(3-(5-oxo-1H,4H-1,2,4-triazolo)methylmorpholine. The pharmaceutical compositions of this invention useful in the treatment or prevention of disorders such as psychiatric disorders including depression and anxiety, inflammatory diseases and emesis.

    Patent expiration dates:

    • September 26, 2027
      Drug product
    • September 26, 2027
      Drug product
    • September 26, 2027
      Drug product


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.
AB Products meeting necessary bioequivalence requirements. Multisource drug products listed under the same heading (e.g. identical active ingredients, dosage form, and routes of administration) and having the same strength (see Therapeutic Equivalence-Related Terms, Pharmaceutical Equivalents) generally will be coded AB if a study is submitted demonstrating bioequivalence. In certain instances, a number is added to the end of the AB code to make a three character code (e.g. AB1, AB2, AB7). Three-character codes are assigned only in situations when more than one reference listed drug of the same strength has been designated under the same heading. Two or more reference listed drugs are generally selected only when there are at least two potential reference drug products which are not bioequivalent to each other. If a study is submitted that demonstrates bioequivalence to a specific listed drug product, the generic product will be given the same three-character code as the reference listed drug it was compared against.

Further information

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