Ethyol is a brand name of amifostine, approved by the FDA in the following formulation(s):
ETHYOL (amifostine - injectable; injection)
Manufacturer: MEDIMMUNE
Approval date: December 8, 1995
Strength(s): 500MG/VIAL [RLD][AP]
Has a generic version of Ethyol been approved?
A generic version of Ethyol has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Ethyol and have been approved by the FDA:
amifostine injectable; injection
Manufacturer: SUN PHARMA GLOBAL
Approval date: March 14, 2008
Strength(s): 500MG/VIAL [AP]
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Ethyol. 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.
Crystalline amifostine compositions and methods of the preparation and use of same
Patent 5,424,471
Issued: June 13, 1995
Inventor(s): Kennedy; Paul E. & Rajewski; Roger A. & Baldoni; John M.
Assignee(s): U.S. Bioscience, Inc.
The present invention relates to a sterile, stable vacuum dried crystalline amifostine composition and, optionally, pharmaceutically acceptable excipient(s). Typically, the crystalline compositions of the present invention exhibit enhanced stability at temperatures ranging from about 4.degree. C. to about ambient temperature for a period of at least 2 years relative to existing solid vacuum dried amorphous amifostine preparations. The reconstituted compositions of the present invention are suitable for administration to humans as a radio- or chemoprotecting agent.Patent expiration dates:
- July 31, 2012
- July 31, 2012
Crystalline amifostine compositions
Patent 5,591,731
Issued: January 7, 1997
Inventor(s): Kennedy; Paul E. & Rajewski; Roger A. & Baldoni; John M.
Assignee(s): U.S. Bioscience, Inc.
The present invention relates to a sterile, stable vacuum dried crystalline amifostine composition and, optionally, pharmaceutically acceptable excipient(s). Typically, the crystalline compositions of the present invention exhibit enhanced stability at temperatures ranging from about 4.degree. C. to about ambient temperature for a period of at least 2 years relative to existing solid vacuum dried amorphous amifostine preparations. The reconstituted compositions of the present invention are suitable for administration to humans as a radio- or chemoprotecting agent.Patent expiration dates:
- July 31, 2012
- July 31, 2012
Methods for treatment of neuro--and nephro--disorders and therapeutic toxicities using aminothiol compounds
Patent 5,994,409
Issued: November 30, 1999
Inventor(s): Stogniew; Martin & Alberts; David S. & Kaplan; Edward H.
Assignee(s): U.S. Bioscience, Inc.
The Arizona Board of Regents on behalf of the University of Arizona
The present invention relates to new uses of S-2-(3-aminopropylamino)ethyl dihydrogen phosphorothioate, (amifostine) and other aminothiol compounds to treat and reverse toxicities caused by therapeutic agents, radiation treatment or diabetes. In particular, the invention provides a method for treating neurotoxicity and nephrotoxicity associated with the administration of chemotherapeutic agents.Patent expiration dates:
- December 8, 2017✓
- December 8, 2017
See also...
- Ethyol Consumer Information (Wolters Kluwer)
- Ethyol Advanced Consumer Information (Micromedex)
- Ethyol AHFS DI Monographs (ASHP)
- Amifostine Consumer Information (Wolters Kluwer)
- Amifostine Intravenous Advanced Consumer Information (Micromedex)
- Amifostine AHFS DI Monographs (ASHP)
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