Rapamune is a brand name of sirolimus, approved by the FDA in the following formulation(s):
RAPAMUNE (sirolimus - solution; oral)
Manufacturer: WYETH PHARMS INC
Approval date: September 15, 1999
Strength(s): 1MG/ML [RLD]
RAPAMUNE (sirolimus - tablet; oral)
Manufacturer: WYETH PHARMS INC
Approval date: August 25, 2000
Strength(s): 1MG
Manufacturer: WYETH PHARMS INC
Approval date: August 22, 2002
Strength(s): 2MG [RLD]
Manufacturer: WYETH PHARMS INC
Approval date: January 25, 2010
Strength(s): 0.5MG
Has a generic version of Rapamune been approved?
No. There is currently no therapeutically equivalent version of Rapamune available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Rapamune. 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.
Methods of inhibiting transplant rejection in mammals using rapamycin and derivatives and prodrugs thereof
Patent 5,100,899
Issued: March 31, 1992
Inventor(s): Calne; Roy
This invention provides a method of inhibiting organ or tissue transplant rejection in a mammal in need thereof, comprising administering to said mammal a transplant rejection inhibiting amount of rapamycin. Also disclosed is a method of inhibiting organ or tissue transplant rejection in a mammal in need thereof, comprising administering to said mammal (a) an amount of rapamycin in combination with (b) an amount of one or more other chemotherapeutic agents for inhibiting transplant rejection, e.g., azathioprine, corticosteroids, cyclosporin and FK506, said amounts of (a) and (b) together being effective to inhibit transplant rejection and to maintain inhibition of transplant rejection.Patent expiration dates:
- July 7, 2013✓
- January 7, 2014✓
- July 7, 2013
Surface modified drug nanoparticles
Patent 5,145,684
Issued: September 8, 1992
Inventor(s): Liversidge; Gary G. & Cundy; Kenneth C. & Bishop; John F. & Czekai; David A.
Assignee(s): Sterling Drug Inc.
Dispersible particles consisting essentially of a crystalline drug substance having a surface modifier adsorbed on the surface thereof in an amount sufficient to maintain an effective average particle size of less than about 400 nm, methods for the preparation of such particles and dispersions containing the particles. Pharmaceutical compositions containing the particles exhibit unexpected bioavailability and are useful in methods of treating mammals.Patent expiration dates:
- July 25, 2011✓
- July 25, 2011
Methods of inhibiting transplant rejecton in mammals using rapamycin and derivatives and prodrugs thereof
Patent 5,403,833
Issued: April 4, 1995
Inventor(s): Calne; Sir Roy
This invention provides a method of inhibiting organ or tissue transplant rejection in a mammal in need thereof, comprising administering to said mammal a transplant rejection inhibiting amount of rapamycin. Also disclosed is a method of inhibiting organ or tissue transplant rejection in a mammal in need thereof, comprising administering to said mammal (a) an amount of rapamycin in combination with (b) an amount of one or more other chemotherapeutic agents for inhibiting transplant rejection, e.g., azathioprine, corticosteroids, cyclosporin and FK506, said amounts of (a) and (b) together being effective to inhibit transplant rejection and to maintain inhibition of transplant rejection.Patent expiration dates:
- April 4, 2012✓
- October 4, 2012✓
- April 4, 2012
Rapamycin formulations for oral administration
Patent 5,536,729
Issued: July 16, 1996
Inventor(s): Waranis; Robert P. & Leonard; Thomas W.
Assignee(s): American Home Products Corporation
The present invention provides novel oral rapamycin formulations which have, per 100 ml of the formulation, from about 0.01 grams to about 5.0 grams of rapamycin, from about 0.05% to about 10% by volume of surfactant, and from about 75% to about 99.95% by volume of a solution of phospholipid or lecithin in which the phospholipid or lecithin therein is 40% to 75% by weight.Patent expiration dates:
- September 30, 2013✓
- March 30, 2014✓
- September 30, 2013
Rapamycin formulations for oral administration
Patent 5,989,591
Issued: November 23, 1999
Inventor(s): Nagi; Arwinder S.
Assignee(s): American Home Products Corporation
This invention provides rapamycin solid dosage unit which comprises a core and a sugar overcoat, said sugar overcoat comprising rapamycin, one or more surface modifying agents, one or more sugars, and optionally one or more binders.Patent expiration dates:
- March 11, 2018✓
- September 11, 2018✓
- March 11, 2018
See also...
- Rapamune Consumer Information (Wolters Kluwer)
- Rapamune Solution Consumer Information (Wolters Kluwer)
- Rapamune Consumer Information (Cerner Multum)
- Rapamune Advanced Consumer Information (Micromedex)
- Rapamune AHFS DI Monographs (ASHP)
- Sirolimus Consumer Information (Wolters Kluwer)
- Sirolimus Solution Consumer Information (Wolters Kluwer)
- Sirolimus Consumer Information (Cerner Multum)
- Sirolimus Advanced Consumer Information (Micromedex)
- Sirolimus AHFS DI Monographs (ASHP)
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