Adcirca is a brand name of tadalafil, approved by the FDA in the following formulation(s):
ADCIRCA (tadalafil - tablet; oral)
Manufacturer: ELI LILLY CO
Approval date: May 22, 2009
Strength(s): 20MG [RLD]
Has a generic version of Adcirca been approved?
No. There is currently no therapeutically equivalent version of Adcirca available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Adcirca. 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.
Tetracyclic derivatives; process of preparation and use
Patent 5,859,006
Issued: January 12, 1999
Inventor(s): Daugan; Alain Claude-Marie
Assignee(s): ICOS Corporation
A compound of formula (I) ##STR1## and salts and solvates thereof, in which: R.sup.0 represents hydrogen, halogen or C.sub.1-6 alkyl; R.sup.1 represents hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, haloC.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.3-8 cycloalkylC.sub.1-3 alkyl, arylC.sub.1-3 alkyl or heteroarylC.sub.1-3 alkyl; R.sup.2 represents an optionally substituted monocyclic aromatic ring selected from benzene, thiophene, furan and pyridine or an optionally substituted bicyclic ring ##STR2## attached to the rest of the molecule via one of the benzene ring carbon atoms and wherein the fused ring A is a 5- or 6-membered ring which may be saturated or partially or fully unsaturated and comprises carbon atoms and optionally one or two heteroatoms selected from oxygen, sulphur and nitrogen; and R.sup.3 represents hydrogen or C.sub.1-3 alkyl, or R.sup.1 and R.sup.3 together represent a 3- or 4-membered alkyl or alkenyl chain. A compound of formula (I) is a potent and selective inhibitor of cyclic guanosine 3', 5'-monophosphate specific phosphodiesterase (cGMP specific PDE) having a utility in a variety of therapeutic areas where such inhibition is beneficial, including the treatment of cardiovascular disorders.Patent expiration dates:
- November 21, 2017✓✓✓
- November 21, 2017
Beta-carboline drug products
Patent 6,821,975
Issued: November 23, 2004
Inventor(s): Neil R.; Anderson & Kerry J.; Hartauer & Martha A.; Kral & Gregory A.; Stephenson
Assignee(s): Lilly ICOS LLC
A compound of structural formula (I), and pharmaceutically acceptable salts and solvates thereof, wherein the compound is in free drug particulate form, is disclosed.Patent expiration dates:
- November 19, 2020✓✓
- November 19, 2020
β-carboline pharmaceutical compositions
Patent 7,182,958
Issued: February 27, 2007
Inventor(s): Oren; Peter L. & Anderson; Neil R. & Kral; Martha A.
Assignee(s): Lilly Icos LLC.
Formulations containing a PDE5 inhibitor, a water-soluble diluent, a lubricant, a hydrophilic binder, a disintegrant, and optional microcrystalline cellulose and/or a wetting agent, and their use in treating sexual dysfunction, are disclosed.Patent expiration dates:
- April 26, 2020✓
- April 26, 2020
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:
- May 22, 2012 - NEW PRODUCT
- May 22, 2016 - ORPHAN DRUG EXCLUSIVITY
See also...
- Adcirca Consumer Information (Drugs.com)
- Adcirca Consumer Information (Wolters Kluwer)
- Adcirca Consumer Information (Cerner Multum)
- Adcirca Advanced Consumer Information (Micromedex)
- Tadalafil Consumer Information (Drugs.com)
- Tadalafil Consumer Information (Wolters Kluwer)
- Tadalafil Consumer Information (Cerner Multum)
- Tadalafil Advanced Consumer Information (Micromedex)
- Tadalafil AHFS DI Monographs (ASHP)
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