Abstract: Provided are a method for making (±)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolenecarboxylic acid, commonly known as gatifloxacin, in high purity, in a suspension in a dipolar aprotic solvent.
Type:
Grant
Filed:
August 14, 2003
Date of Patent:
May 12, 2009
Assignee:
Teva Pharmaceuticals USA, Inc.
Inventors:
Valerie Niddam-Hildesheim, Ben-Zion Dolitzky, Gideon Pilarski, Greta Sterimbaum
Abstract: Vaginal pharmaceutical compositions are described. These compositions contain (i) an active pharmaceutical ingredient selected from the group consisting of antimicrobial imidazoles and mixtures thereof, and (ii) a polysaccharide, wherein the pH of the composition is greater than 4.25 and less than about 8. In particularly preferred compositions, the active pharmaceutical ingredient includes metronidazole and the polysaccharide includes hypromellose. These compositions can be applied to vaginal tissue for treatment of various diseases, such as bacterial vaginosis, or for prophylaxis.
Abstract: This invention relates to an improved process of preparing carvedilol, as well as a new crystalline hydrate and solvate and forms of carvedilol, processes for the manufacture thereof, and pharmaceutical compositions thereof.
Type:
Application
Filed:
April 15, 2008
Publication date:
August 14, 2008
Applicants:
Teva Pharmaceutical Industries Ltd., Teva Pharmaceuticals USA, Inc.
Inventors:
Jean Hildesheim, Sergey Finogueev, Judith Aronhime, Ben-Zion Dolitzky, Shoshana Ben-Valid, Ilan Kor
Abstract: Provided are novel crystalline forms of gatifloxacin, denominated forms L, M, P, Q, S, and T1, and methods for making them. Also provided are methods of transforming the novel crystalline forms of gatifloxacin of the present invention to other crystalline forms of gatifloxacin.
Type:
Grant
Filed:
August 6, 2003
Date of Patent:
July 8, 2008
Assignee:
Teva Pharmaceuticals USA, Inc.
Inventors:
Valerie Niddam-Hildesheim, Shlomit Wizel, Greta Sterimbaum
Abstract: A process for preparing indanylamine and aminotetralin derivatives from indanone or tetralone oximes by acylating the oximes with an organic anhydride, followed by catalytic hydrogenation in the presence of an organic anhydride with subsequent hydrolysis is described. The process is commercially feasible providing indanylamine and aminotetralin derivatives in high yield that are useful as intermediates in the production of therapeutically active compounds. Also described are novel intermediates, 1-indanone O-acetyl oximes and 1-tetralone O-acetyl oximes.
Abstract: Stabilized bupropion hydrochloride pharmaceutical compositions are disclosed that are free of acid additives and provide for a sustained release of the bupropion hydrochloride. The particulate bupropion hydrochloride may be coated with a membrane coating and large-size particles may also be used. Methods for treating individuals using the stabilized bupropion hydrochloride pharmaceutical compositions are also provided.
Abstract: Hydrophillic compositions and methods of use are provided for debriding and wound healing applications. The compositions contain certain proteases produced by microorganisms of the genus Vibrio.
Type:
Grant
Filed:
June 2, 1997
Date of Patent:
January 25, 2000
Assignees:
W. R. Grace & Co., Conn. / Teva Pharmaceuticals USA, Inc.
Inventors:
Donald Zane Fortney, Donald Richard Durham, Kang Yang