Generic Fanapt Availability
FANAPT (iloperidone - tablet;oral)
Approval date: May 6, 2009
Strength(s): 1MG [RLD], 2MG, 4MG, 6MG, 8MG, 10MG, 12MG
Has a generic version of Fanapt been approved?
No. There is currently no therapeutically equivalent version of Fanapt available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Fanapt. 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.
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.
Methods for the administration of iloperidone
Issued: November 19, 2013
Assignee(s): Vanda Pharmaceuticals, Inc.
The present invention relates to methods for the identification of genetic polymorphisms that may be associated with a risk for QT prolongation after treatment with iloperidone and related methods of administering iloperidone to patients with such polymorphisms.Patent expiration dates:
- November 2, 2027✓
- November 2, 2027
Heteroarylpiperidines, pyrrolidines and piperazines and their use as antipsychotics and analgesics
Issued: July 18, 2006
Inventor(s): Strupczewski; Joseph T. & Helsley; Grover C. & Chiang; Yulin & Bordeau; Kenneth J. & Glamkowski; Edward J.
Assignee(s): Aventis Pharmaceuticals Inc.
Heteroarylpiperidines, pyrrolidines, and piperazines are useful as antipsychotic and analgesic agents. The compounds are especially useful for treating psychoses by administering to a mammal a psychoses-treating effective amounts of one of the compounds. The compounds are also useful as analgesics by administering a pain-relieving effective amount of one of the compounds to a mammal.Patent expiration dates:
- November 15, 2016✓✓✓
- November 15, 2016
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:
- May 6, 2014 -
- Fanapt Consumer Information (Drugs.com)
- Fanapt Consumer Information (Wolters Kluwer)
- Fanapt Consumer Information (Cerner Multum)
- Fanapt Advanced Consumer Information (Micromedex®)
- Fanapt Titration Pack Advanced Consumer Information (Micromedex®)
- Fanapt AHFS DI Monographs (ASHP)
- Iloperidone Consumer Information (Wolters Kluwer)
- Iloperidone Consumer Information (Cerner Multum)
- Iloperidone Advanced Consumer Information (Micromedex®)
- Iloperidone AHFS DI Monographs (ASHP)
- Iloperidonesee AHFS DI Monographs (ASHP)
|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.|