Generic Delatestryl Availability

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

DELATESTRYL (testosterone enanthate - injectable;injection)

  • Manufacturer: ENDO PHARMS
    Approved Prior to Jan 1, 1982
    Strength(s): 200MG/ML [RLD] [AO]

Has a generic version of Delatestryl been approved?

Yes. The following products are equivalent to Delatestryl:

testosterone enanthate injectable;injection

  • Manufacturer: HIKMA FARMACEUTICA
    Approval date: September 18, 2012
    Strength(s): 200MG/ML [AO]
  • Manufacturer: MYLAN INSTITUTIONAL
    Approval date: October 5, 2009
    Strength(s): 200MG/ML [AO]
  • Manufacturer: PADDOCK LLC
    Approval date: June 14, 2006
    Strength(s): 200MG/ML [AO]
  • Manufacturer: WATSON LABS
    Approved Prior to Jan 1, 1982
    Strength(s): 200MG/ML [AO]

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

There are no current U.S. patents associated with Delatestryl.

Glossary

TermDefinition
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.
AOInjectable oil solutions. The absorption of drugs in injectable (parenteral) oil solutions may vary substantially with the type of oil employed as a vehicle and the concentration of the active ingredient. Injectable oil solutions are therefore considered to be pharmaceutically and therapeutically equivalent only when the active ingredient, its concentration, and the type of oil used as a vehicle are all identical.
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