Zavesca is a brand name of miglustat, approved by the FDA in the following formulation(s):
ZAVESCA (miglustat - capsule; oral)
Manufacturer: ACTELION PHARMS LTD
Approval date: July 31, 2003
Strength(s): 100MG [RLD]
Has a generic version of Zavesca been approved?
No. There is currently no therapeutically equivalent version of Zavesca available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Zavesca. 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.
Method of inhibiting glycolipid synthesis
Patent 5,472,969
Issued: December 5, 1995
Inventor(s): Platt; Frances M. & Neises; Gabrielle R. & Dwek; Raymond A. & Butters; Terry D.
Assignee(s): Monsanto Company
A method is disclosed for inhibiting the biosynthesis of glycolipids in cells capable of producing glycolipids comprising subjecting said cells to a glycolipid inhibitory effective amount of an N-alkyl derivative of 1,5-dideoxy-1,5-imino-D-glucitol in which said alkyl contains from 2-8 carbon atoms.Patent expiration dates:
- May 13, 2013
- May 13, 2013
Method of inhibiting glycolipid synthesis
Patent 5,525,616
Issued: June 11, 1996
Inventor(s): Platt; Frances M. & Neises; Gabrielle R. & Dwek; Raymond A. & Butters; Terry D.
Assignee(s): Monsanto Company
A method is disclosed for inhibiting the biosynthesis of glycolipids in cells capable of producing glycolipids comprising subjecting said cells to a glycolipid inhibitory effective amount of an N-alkyl derivative of 1,5-dideoxy-1,5-imino-D-glucitol in which said alkyl contains from 2-8 carbon atoms.Patent expiration dates:
- June 11, 2013
- June 11, 2013
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:
- July 31, 2010 - ORPHAN DRUG EXCLUSIVITY
See also...
- Zavesca Consumer Information (Drugs.com)
- Zavesca Consumer Information (Wolters Kluwer)
- Zavesca Consumer Information (Cerner Multum)
- Zavesca Advanced Consumer Information (Micromedex)
- Zavesca AHFS DI Monographs (ASHP)
- Miglustat Consumer Information (Wolters Kluwer)
- Miglustat Consumer Information (Cerner Multum)
- Miglustat Advanced Consumer Information (Micromedex)
- Miglustat AHFS DI Monographs (ASHP)
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