See also: Generic Maxalt-MLT
Maxalt is a brand name of rizatriptan, approved by the FDA in the following formulation(s):
MAXALT (rizatriptan benzoate - tablet; oral)
Manufacturer: MERCK
Approval date: June 29, 1998
Strength(s): EQ 10MG BASE [RLD], EQ 5MG BASE
Has a generic version of Maxalt been approved?
No. There is currently no therapeutically equivalent version of Maxalt available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Maxalt. 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.
Triazole containing indole derivatives
Patent 5,298,520
Issued: March 29, 1994
Inventor(s): Baker; Raymond & Matassa; Victor G. & Street; Leslie J.
Assignee(s): Merck Sharp & Dohme Limited
A class of substituted imidazole, triazole and tetrazole derivatives are selective agonists of 5-HT.sub.1 -like receptors and are therefore useful in the treatment of clinical conditions, in particular migraine and associated disorders, for which a selective agonist of these receptors is indicated.Patent expiration dates:
- June 29, 2012✓✓✓
- December 29, 2012✓
- June 29, 2012
Imidazole, triazole and tetrazole derivatives
Patent 5,602,162
Issued: February 11, 1997
Inventor(s): Baker; Raymond & Matassa; Victor G. & Street; Leslie J.
Assignee(s): Merck, Sharp & Dohme Ltd.
A class of substituted imidazole, triazole and tetrazole derivatives are selective agonists of 5-HT.sub.1 -like receptors and are therefore useful in the treatment of clinical conditions, in particular migraine and associated disorders, for which a selective agonist of these receptors is indicated.Patent expiration dates:
- February 11, 2014✓
- August 11, 2014✓
- February 11, 2014
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:
- December 15, 2014 - NEW PATIENT POPULATION
- June 15, 2015 - PEDIATRIC EXCLUSIVITY
See also...
- Maxalt Consumer Information (Drugs.com)
- Maxalt Consumer Information (Wolters Kluwer)
- Maxalt Consumer Information (Cerner Multum)
- Maxalt Advanced Consumer Information (Micromedex)
- Maxalt AHFS DI Monographs (ASHP)
- Rizatriptan Consumer Information (Wolters Kluwer)
- Rizatriptan Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
- Rizatriptan Consumer Information (Cerner Multum)
- Rizatriptan Advanced Consumer Information (Micromedex)
- Rizatriptan Benzoate AHFS DI Monographs (ASHP)
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