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Levitra expired

Levitra is a levitra expired brand name of vardenafil, approved by the FDA in the following formulation(s levitra (vardenafil hydrochloride - tablet;oral manufacturer: bayer hlthcare, approval date: August 19, 2003. Strength(s.5MG, rLD, 5MG, rLD, 10MG, rLD, 20MG. RLD, has a generic version of Levitra been approved? There is currently no therapeutically equivalent version of Levitra available in the United States. Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Levitra. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are levitra expired 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: Generic Drug FAQs. Related Patents, patents are granted by the.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims. 2-phenyl substituted imidazotriazinones as levitra expired phosphodiesterase inhibitors. Patent 6,362,178, issued: March 26, 2002, inventor(s Ulrich; Niew ouml;hner Mazen; Es-Sayed Helmut; Haning Thomas; Schenke Karl-Heinz; Schlemmer J ouml;rg; Keldenich Erwin; Bischoff Elisabeth; Perzborn Klaus; Dembowsky Peter; Serno Marc; Nowakowski. Assignee(s Bayer Aktiengesellschaft, the 2-phenyl-substituted imidazotriazinones having short, unbranched alkyl radicals in the 9-position are prepared from the corresponding 2-phenyl-imidazotriazinones by chlorosulphonation and subsequent reaction with the amines. The compounds inhibit cGMP-metabolizing phosphodiesterases and are suitable for use as active compounds in pharmaceuticals, for the treatment levitra expired of cardiovascular and cerebrovascular disorders and/or disorders of the urogenital system, in particular for the treatment of erectile dysfunction. Patent expiration dates: October 31, 2018, patent use: erectile dysfunction. Drug substance, drug product 2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors. Patent 7,696,206, issued: April 13, 2010, inventor(s Niew #xf6;hner; Ulrich Es-Sayed; Mazen Haning; Helmut levitra expired Schenke; Thomas Schlemmer; Karl-Heinz Keldenich; Jorg Bischoff; Erwin Perzborn; Elisabeth Dembowsky; Klaus Serno; Peter levitra expired Nowakowski; Marc. Assignee(s Bayer Schering Pharma Aktiengesellschaft, the application claims a compound of the formula or a salt, a hydrate, or a hydrate of a salt thereof. The compounds inhibit cGMP-metabolizing phosphodiesterases and are suitable for use as active compounds in pharmaceuticals, for the treatment of erectile dysfunction. Drug substance Drug product Medicaments containing vardenafil hydrochloride trihydrate levitra expired Patent 8,273,876 Issued: September 25, 2012 Inventor(s Serno; Peter Grunenberg; Alfons Ohm; Andreas Bellinghausen; Rainer Vollers; Eimer Henck; Jan-Olav Assignee(s Bayer Intellectual Property GmbH The invention relates to a method for producing medicaments that contain vardenafil. Patent expiration dates: July 23, 2027 Patent use: treatement OF erectiile dysfunction BY administerinilm-coated tablet Medicaments containing vardenafil hydrochloride trihydrate Patent 8,841,446 Issued: September 23, 2014 Assignee(s Bayer Intellectual Property GmbH The invention relates to a method for producing medicaments that contain vardenafil hydrochloride, essentially. Patent expiration dates: July 3, 2023 Drug product Add to My Med List More about Levitra (vardenafil) Consumer resources Other brands: Staxyn Professional resources Related treatment guides Glossary Term Definition Drug Patent A drug patent is assigned by the.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can. Drug Exclusivity Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant. RLeference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (anda).

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