Patents by Inventor Ninad Deshpanday
Ninad Deshpanday has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).
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Publication number: 20240335374Abstract: The present disclosure provides for nasal compositions for antihypertensive drugs and methods for preparing the compositions. The compositions of the disclosure are particularly suitable for pediatric and geriatric populations, and patients with dysphagia, for treatment of conditions and diseases associated with hypertension, essential hypertension, hypertensive crisis, hypertensive emergency, hypertensive urgency, and other cardiovascular disease by administration, via nasal mucosa.Type: ApplicationFiled: October 19, 2023Publication date: October 10, 2024Inventors: Ninad Deshpanday, David M. Oakley, John R. Cardinal, William C. Stagner, Jayaram Reddy Thimmapuram
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Patent number: 8623921Abstract: Disclosed herein are compositions comprising a compound represented by structural formula (I): 2 g of which is reconstitutable in 10 mL of a water in less than 10 minutes, and methods for preparing these compositions. Also disclosed are compositions comprising a compound represented by structural formula (I) and a pharmaceutically acceptable excipient, wherein the molar ratio of said compound to said excipient is from 1:20 to 1:1, and methods for preparing these compositions.Type: GrantFiled: July 15, 2011Date of Patent: January 7, 2014Assignee: Synta Pharmaceuticals Corp.Inventors: Walter J. Lunsmann, Ninad Deshpanday
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Patent number: 8440223Abstract: A sustained release dosage form comprising Quetiapine or a pharmaceutically acceptable salt, polymorphs, solvates, hydrates thereof and one or more non-gellable release controlling polymer and one or more pharmaceutically acceptable excipient(s). A sustained release dosage form comprising first granulation comprising Quetiapine or its pharmaceutically acceptable salts, polymorphs, solvates, hydrates thereof and one or more release controlling material; and second granulation comprising one or more release controlling material which is the same or different than the one or more release controlling material of the first granulation and optionally quetiapine or its pharmaceutically acceptable salts, polymorphs, solvates, hydrates thereof. A method of preparing the sustained release dosage form by first and second granulation followed by milling; blending the said milled granules after second granulation with lubricant followed by compression to form a sustained release dosage form.Type: GrantFiled: June 29, 2009Date of Patent: May 14, 2013Assignee: Lupin LimitedInventors: Avinash Krishnaji Velhal, Sunil Anantrao Mirajkar, Virendra Ramkrupal Kuril, Vineeth Raghavan, Ninad Deshpanday
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Publication number: 20130115246Abstract: The invention relates to reduced dose oral pharmaceutical composition of fenofibrate which exhibits substantial bioequivalence to Antara® Capsules under fasting condition and also capable of reducing the food effect on bioavailability of fenofibrate. Provided is a pharmaceutical composition comprising about 90 mg of fenofibrate particles having a D90 particle size of less than about 600 nm and a pharmaceutically acceptable carrier, wherein the pharmaceutical composition is a solid dosage form suitable for oral administration and is substantially free of food effect such that when administered orally to a human provides an AUC0-t value for fenofibric acid in the blood plasma of the human under a fed state which is higher than the AUC0-t value under a fasted state by up to 12%, wherein t is 96 hours from the administration of the pharmaceutical composition.Type: ApplicationFiled: January 13, 2012Publication date: May 9, 2013Applicant: Lupin Atlantis Holdings, S.A.Inventors: Venkat Reddy KALLEM, Raghu Rami Reddy KASU, Subhasis DAS, Vijaya Kumar THOMMANDRU, Ninad DESHPANDAY
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Publication number: 20120027855Abstract: The present invention relates to controlled release pharmaceutical formulations of active principle(s) like tetracycline-class antibiotics for providing increased residence time in the gastrointestinal tract and the process of preparing them.Type: ApplicationFiled: August 1, 2011Publication date: February 2, 2012Applicant: Lupin LimitedInventors: Ashish Ashokrao DESHMUKH, Pravin Meghrajji Bhutada, Sajeev Chandran, Thommandru Vijaya Kumar, Shirishkumar Kulkarni, Ninad Deshpanday
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Publication number: 20110294895Abstract: Disclosed herein are compositions comprising a compound represented by structural formula (I): 2 g of which is reconstitutable in 10 mL of a water in less than 10 minutes, and methods for preparing these compositions. Also disclosed are compositions comprising a compound represented by structural formula (I) and a pharmaceutically acceptable excipient, wherein the molar ratio of said compound to said excipient is from 1:20 to 1:1, and methods for preparing these compositions.Type: ApplicationFiled: July 15, 2011Publication date: December 1, 2011Applicant: Synta Pharmaceuticals Corp.Inventors: Walter J. LUNSMANN, Ninad DESHPANDAY
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Publication number: 20110151002Abstract: A sustained release dosage form comprising Quetiapine or a pharmaceutically acceptable salt, polymorphs, solvates, hydrates thereof and one or more non-gellable release controlling polymer and one or more pharmaceutically acceptable excipient(s). A sustained release dosage form comprising first granulation comprising Quetiapine or its pharmaceutically acceptable salts, polymorphs, solvates, hydrates thereof and one or more release controlling material; and second granulation comprising one or more release controlling material which is the same or different than the one or more release controlling material of the first granulation and optionally quetiapine or its pharmaceutically acceptable salts, polymorphs, solvates, hydrates thereof. A method of preparing the sustained release dosage form by first and second granulation followed by milling; blending the said milled granules after second granulation with lubricant followed by compression to form a sustained release dosage form.Type: ApplicationFiled: June 29, 2009Publication date: June 23, 2011Applicant: LUPIN LIMITEDInventors: Avinash Krishnaji Velhal, Sunil Anantrao Mirajkar, Virendra Ramkrupal Kuril, Vineeth Raghavan, Ninad Deshpanday
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Publication number: 20100249239Abstract: Disclosed herein are compositions comprising a compound represented by structural formula (I): 2 g of which is reconstitutable in 10 mL of a water in less than 10 minutes, and methods for preparing these compositions. Also disclosed are compositions comprising a compound represented by structural formula (I) and a pharmaceutically acceptable excipient, wherein the molar ratio of said compound to said excipient is from 1:20 to 1:1, and methods for preparing these compositions.Type: ApplicationFiled: February 1, 2010Publication date: September 30, 2010Inventors: Walter J. Lunsmann, Ninad Deshpanday
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Patent number: 7678832Abstract: Disclosed herein are compositions comprising a compound represented by structural formula (I): 2 g of which is reconstitutable in 10 mL of a water in less than 10 minutes, and methods for preparing these compositions. Also disclosed are compositions comprising a compound represented by structural formula (I) and a pharmaceutically acceptable excipient, wherein the molar ratio of said compound to said excipient is from 1:20 to 1:1, and methods for preparing these compositions.Type: GrantFiled: August 10, 2006Date of Patent: March 16, 2010Assignee: Synta Pharmaceuticals Corp.Inventors: Walter J. Lunsmann, Ninad Deshpanday
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Publication number: 20070088057Abstract: Disclosed herein are compositions comprising a compound represented by structural formula (I): 2 g of which is reconstitutable in 10 mL of a water in less than 10 minutes, and methods for preparing these compositions. Also disclosed are compositions comprising a compound represented by structural formula (I) and a pharmaceutically acceptable excipient, wherein the molar ratio of said compound to said excipient is from 1:20 to 1:1, and methods for preparing these compositions.Type: ApplicationFiled: August 10, 2006Publication date: April 19, 2007Inventors: Walter Lunsmann, Ninad Deshpanday
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Patent number: 5834010Abstract: A composition and method for enhancing transdermal penetration of a basic drug are described. The composition comprises a matrix patch comprising an effective amount of a basic drug, preferably having a pK.sub.a of about 8.0 or greater, an effective amount of a penetration enhancer consisting essentially of triacetin, and a polymer layer preferably comprising a pressure-sensitive adhesive. A preferred basic drug is oxybutynin and acid addition salts thereof. The method for enhancing transdermal penetration comprises applying the matrix patch to a selected area of skin.Type: GrantFiled: January 3, 1997Date of Patent: November 10, 1998Assignee: Theratech, Inc.Inventors: Danyi Quan, Ninad A. Deshpanday, Srinivasan Venkateshwaran, Charles D. Ebert
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Patent number: 5601839Abstract: A composition and method for enhancing transdermal penetration of a basic drug are described. The composition comprises a matrix patch comprising an effective amount of a basic drug, preferably having a pK.sub.a of about 8.0 or greater, an effective amount of penetration enhancer consisting essentially of triacetin, and a polymer later preferably comprising a pressure-sensitive adhesive. A preferred basic drug is oxybutynin and acid addition salts thereof. The method for enhancing transdermal penetration comprises applying the matrix patch to a selected area of skin.Type: GrantFiled: April 26, 1995Date of Patent: February 11, 1997Assignee: TheraTech, Inc.Inventors: Danyi Quan, Ninad A. Deshpanday, Srinivasan Venkateshwaran, Charles D. Ebert