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Deshpande, IN
Amit Deshpande, Mumbai IN
| Patent application number | Description | Published |
|---|---|---|
| 20100010002 | ANTICANCER USE OF CAFFEIC ACID AND ITS DERIVATIVES - The present invention relates to the use of caffeic acid or a derivative thereof represented by the following general formula (1) | 01-14-2010 |
Anil Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20100310493 | ACETAMIDE DERIVATIVES AS GLUCOKINASE ACTIVATORS, THEIR PROCESS AND MEDICINAL APPLICATION - Acetamide derivatives, their stereoisomers, tautomers, prodrugs, pharmaceutically acceptable salts, polymorphs, solvates and formulations thereof for the prophylaxis, management, treatment, control of progression, or adjunct treatment of diseases and/or medical conditions where the activation of glucokinase would be beneficial, are disclosed. | 12-09-2010 |
Anjali Apte Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20110165583 | VECTOR FOR IDENTIFICATION, SELECTION AND EXPRESSION OF RECOMBINANTS - A modified vector comprising a reporter gene having a STOP codon upstream of the multiple cloning site of the vector which is characterized in that the recombinant clones show fluoresce or show color in presence of inducer. A method for identification and selection of recombinant clones comprising the modified vector wherein the recombinant clones florescence or show color in a suitable suppressor strain of the STOP codon associated with the gene of interest. A method of preparation of recombinant clone comprising gene of interest and modified vector comprising amplification of gene of interest using specific primers containing STOP codon different from STOP codon used with reporter gene; cloning the amplified gene of interest in the modified vector; transformation of cloned modified vector in the STOP codon suppressor host cell wherein the STOP codon suppressor host cell is specific for STOP codon used with the gene of interest wherein the recombinant clones either fluorescence or show color depending upon the reporter gene used. | 07-07-2011 |
Devendra Ramakant Deshpande, Noida IN
| Patent application number | Description | Published |
|---|---|---|
| 20090282379 | SYSTEM AND METHOD FOR CIRCUIT SCHEMATIC GENERATION - The present invention provides a system and method for generating circuit schematic that includes extracting connectivity data of a plurality of devices from a netlist, categorizing the plurality of devices into groups, placing Schematic Analog Placement Constraints on all the instances by identifying instances among the groups that match with a circuit template (in-built as well as user-specified), creating a BFS instance tree of tree instances, creating a two terminal device clusters and creating instance attachments. Using the constraints during grid based placement and eventually generated schematic which look like analog schematic. | 11-12-2009 |
Dinkar Amol Deshpande, Andra Pradesh IN
| Patent application number | Description | Published |
|---|---|---|
| 20100041669 | 4-(HETEROCYCLYL)ALKYL-N-(ARYLSULFONYL)INDOLE COMPOUNDS AND THEIR USE AS 5-HT6 LIGANDS - Compounds including 4-(Heterocyclyl)alkyl-N-(arylsulfonyl)indole compounds of the formula (I), their derivatives, their stereoisomers, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them as well as a process for the preparation of these compounds, their derivatives, their stereoisomers, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them. These compounds are useful in the treatment of various disorders that are related to 5-HT | 02-18-2010 |
Jayant Deshpande, New Bombay IN
| Patent application number | Description | Published |
|---|---|---|
| 20100112188 | NOVEL STABLE BEADLETS OF LIPOPHILIC NUTRIENTS - The invention disclosed in this application relates to novel stable beadlets of lipophilic nutrients comprising an inert core having a coating of stabilizing antioxidants, lipophilic nutrients, or mixtures thereof. The beadlets may be coated with one or more coatings to protect the lipophilic ingredients from the atmosphere, specifically the coatings can be used to protect against moisture and/or oxygen. The invention also relates to a process for the preparation of the stable beadlets. The beadlets can be used in medicines and dietary supplements intended to facilitate the reduced risk of macular degeneration, cataract, and several forms of cancer. | 05-06-2010 |
Madhuri Deshpande, Mumbai IN
| Patent application number | Description | Published |
|---|---|---|
| 20110173052 | Enhanced Knowledge Management - A knowledge management module associated with an organization hierarchically arranges knowledge relevant to the organization. The knowledge management module may communicate with databases internal and external to the organization to connect individuals to information regarding elements within the map. In certain embodiments, the management server also includes, for each element in the knowledge management map, information related to the levels of expertise of personnel associated with the organization. In another embodiment, the knowledge management module may include processing capabilities that allow it to recompute the links between each element of the map when errors have been found or when new elements need to be added. | 07-14-2011 |
Manoj Madhukarrao Deshpande, Ahmedpur IN
| Patent application number | Description | Published |
|---|---|---|
| 20090198058 | Process for Preparation of Dextrorotatory Isomer of 6-(5- chloro-pyrid-2-yl)-5-[(4-methyl -1-piperazinyl) carbonyloxy] -7-oxo-6,7-dihydro-5H-pyrrolo [3,4-b] pyrazine (Eszopiclone) - Disclosed herein is the process for preparation of 6-(5-chloro-pyrid-2-yl)-5-[(4-methyl-1-piperazinyl)carbonyloxy]-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine (Zopiclone), its resolution to get the dextrorotatory isomer of formula (I) substantially free of R(−) enantiomer and recovery of key raw material i.e. 6-(5-chloro pyrid-2-yl)-5-hydroxy-7-oxo-5,6-dihydropyrrolo[3,4-b]pyrazine from the R-isomer of Zopiclone followed by conversion of the recovered compound to get pure Eszopiclone (I) in high yield and high purity. | 08-06-2009 |
Pandurang Balwant Deshpande, Gujarat IN
| Patent application number | Description | Published |
|---|---|---|
| 20090312538 | PROCESS FOR THE PREPARATION OF SUCRALOSE OF HIGH PURITY - The present invention relates to an improved process for the preparation of Sucralose having purity of at least 99.6% comprising steps of | 12-17-2009 |
| 20100105889 | PROCESS FOR THE PREPARATION OF PENTOSAN POLYSULFATE OR SALTS THEREOF - A process for the preparation of Pentosan polysulfate sodium comprising a step of purifying depolymerized crude Pentosan polysulfate sodium by filtration through NF membrane system. | 04-29-2010 |
| 20100234632 | PROCESS FOR THE PREPARATION OF ENTACAPONE - The present invention relates to an improved process for the preparation of Entacapone of formula (I) | 09-16-2010 |
Pandurang Balwant Deshpande, Mumbai IN
| Patent application number | Description | Published |
|---|---|---|
| 20090124803 | PROCESS FOR PREPARATION OF ROSUVASTATIN - The invention relates to commercially viable process for the preparation of Rosuvastatin by an early introduction of the correct absolute stereochemistry at C-5 (S) of Rosuvastatin side chain followed by regioselective chain extension using novel side chain building blocks. It is yet another object of the invention is to provide novel intermediates that may be used for the preparation of Rosuvastatin. Formula (I). | 05-14-2009 |
Pandurang Balwant Deshpande, Vadodara IN
| Patent application number | Description | Published |
|---|---|---|
| 20100113798 | PROCESS FOR PREPARATION OF IRBESARTAN - A process for the preparation of Irbesartan of formula (I) using the step of, | 05-06-2010 |
| 20100179332 | PROCESS FOR THE PURIFICATION OF ROPINIROLE HYDROCHLORIDE - The present invention provides an improved process for the purification of ropinirole hydrochloride. The process includes (i) treating ropinirole hydrochloride with sodium dithionate and charcoal in suitable alcoholic solvent; (ii) triturating the ropinirole hydrochloride obtained in step (i) with ethanol; (iii) reacting the triturated solid with base in water immiscible solvent and isolating the free base; and (iv) treating the free base obtained in step (iii) with ethanolic HCl to give ropinirole hydrochloride. | 07-15-2010 |
| 20100249433 | PROCESS FOR THE PURIFICATION OF ROPINIROLE HYDROCHLORIDE - An improved process is described for the purification of ropinirole hydrochloride. The process includes (i) dissolving ropinirole hydrochloride in water; (ii) treating the solution obtained in step (i) with sodium dithionate and charcoal; (iii) treating the filtrate obtained in step (ii) with water immiscible solvent and base and isolating the free base; and (iv) treating the free base obtained in step (iii) with ethanolic HCl to give ropinirole hydrochloride. | 09-30-2010 |
Piyush Deshpande, Chhindwara IN
| Patent application number | Description | Published |
|---|---|---|
| 20100281072 | AUTOMATED MIGRATION OF TRANSLATION MAPS FOR USE IN EXCHANGING DOCUMENTS BETWEEN ENTITIES - A method for migrating a legacy translation map to an evolved translation map includes determining an input file structure from input file structure information in the legacy translation map, determining an output file structure from output file structure information in the legacy translation map, and creating an XML binding object representation of source code for the input and output file structure. The method may further include creating an evolved language object representation of translation instructions in the legacy translation map, adding temporary segments to the XML binding object representation for the input file structure, and generating evolved language object representation of instructions to write input data into the temporary segments. The evolved language object representation of translation instructions is then merged into the XML binding object representation. The evolved translation map is then generated as an XML file based on the XML binding object representation resulting from the merging. | 11-04-2010 |
Pramod Narayan Deshpande, Chennai IN
| Patent application number | Description | Published |
|---|---|---|
| 20120095210 | PROCESS FOR THE PREPARATION OF BETA-LACTAM ANTIBIOTIC - The present invention provides a novel process for the preparation of the meropenem trihydrate of formula (I). | 04-19-2012 |
Pramod Narayan Deshpande, Tamilnadu IN
| Patent application number | Description | Published |
|---|---|---|
| 20090264643 | Process for The Preparation of Beta-Lactam Antibiotic - The present invention relates to a process for the preparation of Meropenem of formula (I) in sterile form and also provides an improved process for the preparation of compound of formula (V), which is an important intermediate in the synthesis of Meropenem. | 10-22-2009 |
Prasad Deshpande, Kharadi IN
| Patent application number | Description | Published |
|---|---|---|
| 20120027194 | SYSTEM AND METHOD FOR MANAGING ABRUPT CONTACT DISCONNECTS - Embodiments of the present invention relate to a system and method for managing abrupt contact disconnects. In accordance with one embodiment, there is provided a method for managing abrupt customer call disconnects from an IVR system, dependent upon variations of call disconnect scenarios, the method comprising detecting an abrupt customer call disconnect; storing IVR options selected by customer before the abrupt customer call disconnect; sending an SMS/voice message notification to the customer; receiving customer call re-connection; determining, whether there is status information of an abnormally terminated call corresponding to the customer call re-connection; retrieving status information of the abnormally terminated call; connecting the IVR system to the customer; and providing IVR system options to the customer based upon the particular disconnect scenario. | 02-02-2012 |
Prasad K. Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20090018123 | Oxazolidinones Bearing Antimicrobial Activity Composition and Methods of Preparation - The present invention concerns recombinant DNA's comprising cDNA of genomic RNA of a Salmonidae alphavirus preceded by a spacer sequence, under the control of a suitable promoter. Said recombinant DNA's are useful for obtaining expression vectors, producing recombinant Salmonidae alphavirus, and for obtaining vaccines. | 01-15-2009 |
Prasad Keshav Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20100056581 | Substituted Piperidino Phenyloxazolidinones - The present invention relates to certain substituted piperidino phenyloxazolidinones. Specifically, the invention relates to geminally disubstituted piperidino phenyloxazolidinones having antimicrobial activity with improved pharmacokinetic profile. The invention also relates to processes for the preparation of compounds of the present invention, pharmaceutical compositions containing the compounds of the present invention and the methods for treating or preventing microbial infections using the compounds of the present invention. | 03-04-2010 |
| 20100144735 | SUBSTITUTED PIPERIDINO PHENYLOXAZOLIDINONES HAVING ANTIMICROBIAL ACTIVITY WITH IMPROVED IN VIVO EFFICACY - The present invention provides agents having antimicrobial activity for preventing and treating infectious diseases. Thus, the present invention provides novel substituted piperidino phenyloxazolidinone derivatives, processes for making compounds as well as antimicrobial compositions containing said derivatives as active ingredients and methods of treating bacterial infections with the said derivatives. | 06-10-2010 |
Prasad Keshav Deshpande, Aurangabad IN
| Patent application number | Description | Published |
|---|---|---|
| 20080214608 | New generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments - This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use. | 09-04-2008 |
Prasad M. Deshpande, Mumbai IN
| Patent application number | Description | Published |
|---|---|---|
| 20090271720 | METHOD FOR DERIVING INTELLIGENCE FROM ACTIVITY LOGS - Techniques for segregating one or more logs of at least one multitasking user to derive at least one behavioral pattern of the at least one multitasking user are provided. The techniques include obtaining at least one of at least one action log, configuration information, domain knowledge, at least one task history and open task repository information, correlating the at least one of at least one action log, configuration information, domain knowledge, at least one task history and open task repository information to determine a task associated with each of one or more actions and segregate the one or more logs based on the one or more actions, and using the one or more logs that have been segregated to derive at least one behavioral pattern of the at least one multitasking user. Techniques are also provided for deriving intelligence from at least one activity log of at least one multitasking user to provide information to the at least one user. | 10-29-2009 |
| 20090271800 | SYSTEM AND COMPUTER PROGRAM PRODUCT FOR DERIVING INTELLIGENCE FROM ACTIVITY LOGS - Techniques for segregating one or more logs of at least one multitasking user to derive at least one behavioral pattern of the at least one multitasking user are provided. The techniques include obtaining at least one of at least one action log, configuration information, domain knowledge, at least one task history and open task repository information, correlating the at least one of at least one action log, configuration information, domain knowledge, at least one task history and open task repository information to determine a task associated with each of one or more actions and segregate the one or more logs based on the one or more actions, and using the one or more logs that have been segregated to derive at least one behavioral pattern of the at least one multitasking user. Techniques are also provided for deriving intelligence from at least one activity log of at least one multitasking user to provide information to the at least one user. | 10-29-2009 |
| 20100332492 | RETRIEVAL OF RELEVANT OBJECTS IN A SIMILARITY - Techniques for retrieval of one or more relevant multi-attribute structured objects with respect to a query are provided. The techniques include receiving a query, grouping one or more attributes of one or more objects in a database into one or more groups according to how each bears a relation to the query, and using the one or more attribute groups to produce an output of one or more relevant multi-attribute structured objects in response to the query. | 12-30-2010 |
| 20110055811 | Discovery, Analysis, and Visualization of Dependencies - Product data pertaining to a plurality of products is gathered from a plurality of sources. Dependency information for the plurality of products is extracted from the product data. The dependency information is analyzed to determine dependencies for each product of the plurality of products. The dependencies for each product of the plurality of products are displayed to a user. | 03-03-2011 |
| 20110191762 | MINING DEPENDENCIES FROM DISK IMAGES - Methods and arrangements for automatically finding the dependency of a software product on other software products or components. From an install image or directory, a signature is found by deriving the same from a directory structure of the software. Further, a directory tree structure is built and an approximate sub-tree matching algorithm is applied to find commonalties across software products. | 08-04-2011 |
Prasad Manikarao Deshpande, Mumbai IN
| Patent application number | Description | Published |
|---|---|---|
| 20120123987 | SYSTEMS AND METHODS FOR DYNAMICALLY RECONFIGURING PREDICTIVE ANALYTICS WITHIN WORKFLOWS USING SELECTIVE USER FEEDBACK - Methods and arrangements for managing and enhancing workflow. A work item is accepted and the is routed from a first node to a second node based on a predictive analytics model. The predictive analytics model is validated, and is reconfigured responsive to the validating. | 05-17-2012 |
Rajiv Deshpande, Mumbai IN
| Patent application number | Description | Published |
|---|---|---|
| 20090261531 | Magnetic Seal Assembly - The technical field of the invention relates to magnetic sealing devices used for transfer of torque involving rotating parts. Industries that deal in chemicals and pharmaceutics have a requirement to mix materials such as gases and liquids. This is carried out by mixers and agitators and similar other equipment. All devices involve a shaft that comes out of the body of the equipment, that is to say it pierces the equipment. The location at which the shaft enters the equipment is a potential point of leakage. One of the technical problems that the present invention tackles is that of providing a secure sealing that will reduce leakage. The magnetic seal assembly disclosed in the present invention provides a magnetic sealing device that gives a safe, trouble- free, robust, and leak-proof contactless seal for agitator drives and similar equipment used for industrial scale applications. The device disclosed in the present invention is used for transferring torque in industrial scale agitators wherein large volumes of liquid can be treated without leakage. | 10-22-2009 |
Shailesh Deshpande, Gujarat IN
| Patent application number | Description | Published |
|---|---|---|
| 20100190824 | Novel Substituted Piperidones as HSP Inducers - The present invention relates to novel compounds of formula (I) or (II), their pharmaceutically acceptable salts and their hydrates, solvates, stereoisomers, conformers, tautomers, polymorphs and prodrugs and also pharmaceutically acceptable compositions containing them Wherein R | 07-29-2010 |
Shailesh Deshpande, Gandhinagar IN
| Patent application number | Description | Published |
|---|---|---|
| 20110130414 | NOVEL FUSED THIAZOLO AND OXAZOLO PYRIMIDINONES - The present invention relates to novel compounds, their pharmaceutically acceptable salts, and their isomers, stereoisomers, conformers, tautomers, polymorphs, hydrates and solvates. The present invention also encompasses pharmaceutically acceptable compositions of said compounds and process for preparing novel compounds. The invention further relates to the use of the above-mentioned compounds for the preparation of medicament for use as pharmaceuticals. | 06-02-2011 |
| 20120046317 | NOVEL HETEROCYCLIC COMPOUNDS - The present invention relates to a new class of heterocyclic compounds and pharmaceutically acceptable salts thereof, process for preparing the same, pharmaceutical composition containing these compounds and to their use in treatment of diseases caused due to formation and accumulation of AGEs (Advanced Glycation end products). The compounds of the present invention are useful for the treatment of diabetic and aging-related complications caused by formation and accumulation of AGEs, such as neuropathy, nephropathy, microangiopathy, retinopathy, hypertension, heart failure, atherosclerosis, Alzheimer's disease & dermatological disorders. | 02-23-2012 |
Smita Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20090024659 | AUTOMATION TOOL FOR PROVIDING ACCESS TO AN ELECTRONIC DATABASE FOR BUSINESS INTELLIGENCE - A method for providing access to an electronic database for business intelligence is provided. The method includes receiving a request to create a new universe to interface with the electronic database to access the electronic database for business intelligence, receiving an input of a first set of universe details to populate the new universe, executing at least a first application macro to populate the new universe with the received first set of universe details by calling a business intelligence application to create the new universe with the populated first set of universe details; and providing the created new universe as a metadata layer that interfaces with the electronic database to provide access to the electronic database. | 01-22-2009 |
Supreet K. Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20100010955 | Molecule Fragmentation Scheme and Method for Designing New Molecules - Group based QSAR method (G-QSAR) is reported which uses descriptors evaluated only for the substituent groups or molecular fragments rather than whole molecule for generating QSAR. In addition, cross terms are calculated from product of descriptors at different substituent sites or fragments and used as descriptors to improve the QSAR models. This method provides QSAR models with predictive ability similar or better to conventional methods and in addition provides hints for sites or fragments of improvement in the molecules. The descriptor ranges for substituents or fragments are used to search for new groups/fragments leading to design of novel molecules with improved activity/property. | 01-14-2010 |
Tushar Ramchandra Deshpande, Maharashtra IN
| Patent application number | Description | Published |
|---|---|---|
| 20090203937 | PROCESS FOR PREPARING L- (+) -LACTIC ACID - The present invention provides a commercially viable process for the preparation of highly pure and optically active L-(+)-lactic acid and S-(−)-methyl lactate, in high yield, obtained from esterification of aqueous crude lactic acid solution produced by sugar cane juice fermentation broth and methanol in continuous counter current trickle phase approach or in continuous counter current bubble column manner, using stabilizers and the methyl lactate so obtained is recovered and followed by purification of reasonably pure methyl lactate using reagent mixture such as sodium bi-carbonate, mono-ethanolamine or di-ethanolamine, urea or sodium-bicarbonate, mono-ethanolamine or di-ethanolamine, thiourea to reduce the impurity of dimethyl ester of dicarboxylic such as dimethyl oxalate or di-methyl succinate or methyl ester of mono-carboxylic acid such as methyl pyruvate present as an impurity, so as to get highly pure S-(−)-methyl lactate followed by hydrolyzing highly pure S-(−)-methyl lactate using highly pure lactic acid as a catalyst, using highly pure water as the hydrolysis media and by using pre-treated activated carbon with dilute L-(+)-lactic acid, in batch or continuous mode. This very high pure S-(−)-methyl lactate constitutes an important product having interesting possibilities of application at an industrial level, in pharmaceuticals. Highly pure L-(+)-lactic acid thus obtained is used as an acidulant, as a food additive, for pharmaceutical applications, a monomer for making poly-lactic acid, as a monomer to prepare biodegradable polymer which are useful for manufacturing bags, application films, in the field of sanitary field, and has medical applications. | 08-13-2009 |
Venkatesh Deshpande, Gulbarga IN
| Patent application number | Description | Published |
|---|---|---|
| 20090248973 | System and method for providing address decode and virtual function (VF) migration support in a peripheral component interconnect express (PCIE) multi-root input/output virtualization (IOV) environment - The present invention is a method for providing address decode and Virtual Function (VF) migration support in a Peripheral Component Interconnect Express (PCIE) multi-root Input/Output Virtualization (IOV) environment. The method may include receiving a Transaction Layer Packet (TLP) from the PCIE multi-root IOV environment. The method may further include comparing a destination address of the TLP with a plurality of base address values stored in a Content Addressable Memory (CAM), each base address value being associated with a Virtual Function (VF), each VF being associated with a Physical Function (PF). The method may further include when a base address value included in the plurality of base address values matches the destination address of the TLP, providing the matching base address value to the PCIE multi-root IOV environment by outputting from the CAM the matching base address value. The method may further include constructing a requestor ID for the VF associated with the matching base address value, the requestor ID being based upon the output matching base address value and a bus number for a PF which owns the CAM. | 10-01-2009 |
| 20110219161 | SYSTEM AND METHOD FOR PROVIDING ADDRESS DECODE AND VIRTUAL FUNCTION (VF) MIGRATION SUPPORT IN A PERIPHERAL COMPONENT INTERCONNECT EXPRESS (PCIE) MULTI-ROOT INPUT/OUTPUT VIRTUALIZATION (IOV) ENVIRONMENT - The present invention is a method for providing address decode and Virtual Function (VF) migration support in a Peripheral Component Interconnect Express (PCIE) multi-root Input/Output Virtualization (IOV) environment. The method may include receiving a Transaction Layer Packet (TLP) from the PCIE multi-root IOV environment. The method may further include comparing a destination address of the TLP with a plurality of base address values stored in a Content Addressable Memory (CAM), each base address value being associated with a Virtual Function (VF), each VF being associated with a Physical Function (PF). The method may further include when a base address value included in the plurality of base address values matches the destination address of the TLP, providing the matching base address value to the PCIE multi-root IOV environment by outputting from the CAM the matching base address value. The method may further include constructing a requestor ID for the VF associated with the matching base address value, the requestor ID being based upon the output matching base address value and a bus number for a PF which owns the CAM. | 09-08-2011 |
Yogesh S. Deshpande, Aurangabad IN
| Patent application number | Description | Published |
|---|---|---|
| 20100159003 | PROCESS FOR THE PREPARATION OF A MEDICAMENT COMPRISING VARDENAFIL HYDROCHLORIDE TRIHYDRATE - The present invention relates to a process for the preparation of a medicament containing vardenafil hydrochloride trihydrate in solid form, in which vardenafil hydrochloride trihydrate is processed with suitable pharmaceutical auxiliaries at a temperature of from approx. 20° C. to approx. 45° C. | 06-24-2010 |
