TEVA GYOGYSZERGYAR RESZVENYTARSASAG

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Recent Patents

Patent # Title Filing Date Issue Date Intl Class
7,452,991 Aztreonam .beta. polymorph with very low residual solvent contentMay 17, 04Nov 18, 08[C07D]
7,348,429 Process for purifying N-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-N-ethylacetamide(zalep-lon) and crystalline forms of zaleplon accessible with the processSep 27, 04Mar 25, 08[C07D]
7,232,486 Crystallization and purification of macrolidesMar 31, 04Jun 19, 07[C30B]
7,220,357 Method of purifying macrolidesJul 26, 04May 22, 07[B01D]
7,145,017 Preparation of AztreonamAug 05, 03Dec 05, 06[C07D]
7,102,026 Process for preparing and isolating rac-bicalutamide and its intermediatesJun 25, 03Sep 05, 06[C07C]
6,506,591 Process for the preparation of pseudomonic acid a antibiotic by microbiological methodOct 11, 01Jan 14, 03[C12N]
5,753,695 Flavilium compounds and method of usingMay 19, 94May 19, 98[C07D, A61K]
5,583,105 Oral pharmaceutical preparationMar 31, 95Dec 10, 96[A61K]
5,565,214 Stable therapeutic oil filled soft gelatin capsulesJul 22, 93Oct 15, 96[A61K]

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Expired/Abandoned/Withdrawn Patents

Patent # Title Filing Date Issue/Pub Date Intl Class
2012/0220,655 CRYSTALLINE FORMS OF FESOTERODINE FUMARATE AND FESOTERODINE BASESep 03, 10Aug 30, 12[C07C, A61P, A61K]
7,737,177 Processes for preparing crystalline and amorphous mupirocin calciumNov 06, 02Jun 15, 10[A61K]
7,700,337 Process for constructing strain having compactin hydroxylation abilityJul 10, 07Apr 20, 10[C12N, C07H, C12P]
7,700,752 Process for constructing strain having compactin hydroxylation abilityJul 10, 07Apr 20, 10[C12N, C07H, C12P]
2008/0300,305 METHOD OF PURIFYING PRAVASTATINAug 07, 08Dec 04, 08[A61K]
7,452,692 Method for extracting a macrolide from biomatterMay 12, 04Nov 18, 08[C12N]
7,439,045 pH controlled fermentation process for pseudomonic acid productionJun 21, 02Oct 21, 08[C12P]
7,432,074 Method for extracting a macrolide from biomatterFeb 12, 03Oct 07, 08[C12N]
7,335,772 1H-imidazo [4,5-c] quinolin-4-cyano and 1H-imidazo [4,5-c] quinolin-4-carboxamide intermediatesDec 09, 04Feb 26, 08[C07D]
2007/0238,739 Process for purifying N-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-n-ethylacetamide (zaleplon) and crystalline forms of zaleplon accessible with the processMay 21, 07Oct 11, 07[C07D, A61K]
7,262,218 Forms of pravastatin sodiumAug 09, 05Aug 28, 07[A61K]
2007/0197,633 Novel forms of pravastatin sodiumApr 03, 07Aug 23, 07[A61K]
2007/0117,976 Method of purifying macrolidesJan 17, 07May 24, 07[C07D]
2007/0060,755 Preparation of 1H-imidazo [4,5-C] quinolin-4-amines via 1H-imidazo [4,5-C] quinolin-4-phthalimide intermediatesNov 15, 06Mar 15, 07[C07D]
7,166,721 Preparation of 1H-imidazo[4,5-C] quinolin 4-amines via novel 1H-imidazo[4,5-c] quinolin 4-cyano and 1H-imidazo[4,5-c] quinolin 4-carboxamide intermediatesDec 09, 04Jan 23, 07[C07D]
7,153,967 Preparation of 1H-imidazo [4,5-C] quinolin-4-amines via 1H-imidazo [4,5-C] quinolin-4-phthalimide intermediatesDec 23, 04Dec 26, 06[C07D]
7,098,345 Process for preparing 1,2,3,9-tetrahydro-9-methyl-3-[(2-methyl-1H-imidazol-1-YL)methyl]-4H-carb-azol-4-oneApr 29, 03Aug 29, 06[C07D]
7,078,223 Process for the preparation of pseudomonic acid a antibiotic by microbiological methodNov 12, 02Jul 18, 06[C12N]
7,001,919 Forms of pravastatin sodiumDec 14, 00Feb 21, 06[A61K]
2005/0215,636 Pravastatin sodium substantially free of pravastatin lactone and EPI-pravastatin, and compositions containing sameMay 16, 05Sep 29, 05[C07C, A61K]

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