Exjade is a brand name of deferasirox, approved by the FDA in the following formulation(s):
EXJADE (deferasirox - tablet, for suspension; oral)
Manufacturer: NOVARTIS
Approval date: November 2, 2005
Strength(s): 125MG, 250MG, 500MG [RLD]
Has a generic version of Exjade been approved?
No. There is currently no therapeutically equivalent version of Exjade available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Exjade. 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.
Substituted 3,5-diphenyl-1,2,4-triazoles and their use as pharmaceutical metal chelators
Patent 6,465,504
Issued: October 15, 2002
Inventor(s): René ; Lattmann & Pierre; Acklin
Assignee(s): Novartis AG
The use is described of 3,5-diphenyl-1,2,4-triazoles of the formula I in which R1-R5 are as defined in the description. The compounds have useful pharmaceutical properties and are particularly active as iron chelators. They can be used for the treatment of iron overload in warm-blooded animals.Patent expiration dates:
- April 5, 2019✓✓
- April 5, 2019
Substituted 3,5-diphenyl-1,2,4-triazoles and their use as pharmaceutical metal chelators
Patent 6,596,750
Issued: July 22, 2003
Inventor(s): René ; Lattmann & Pierre; Acklin
Assignee(s): Novartis AG
The use is described of 3,5-diphenyl-1,2,4-triazoles of the formula I in which R1-R5 are as defined in the description. The compounds have useful pharmaceutical properties and are particularly active as iron chelators. They can be used for the treatment of iron overload in warm-blooded animals.Patent expiration dates:
- June 24, 2017✓✓
- June 24, 2017
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:
- November 2, 2010 - NEW CHEMICAL ENTITY
- November 2, 2012 - ORPHAN DRUG EXCLUSIVITY
See also...
- Exjade Consumer Information (Drugs.com)
- Exjade Consumer Information (Wolters Kluwer)
- Exjade Consumer Information (Cerner Multum)
- Exjade Advanced Consumer Information (Micromedex)
- Exjade AHFS DI Monographs (ASHP)
- Deferasirox Consumer Information (Wolters Kluwer)
- Deferasirox Consumer Information (Cerner Multum)
- Deferasirox Advanced Consumer Information (Micromedex)
- Deferasirox AHFS DI Monographs (ASHP)
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