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Glenmark Generics Ltd.

Glenmark Generics Ltd. Patent applications
Patent application numberTitlePublished
20120028045Processes for the Preparation of Indiplon and Intermediates Thereof - The present invention relates to processes for the preparation of indiplon and its polymorphic mixtures.02-02-2012
20120022047PROCESS FOR THE PURIFICATION OF ESLICARBAZEPINE ACETATE - The present invention relates to the purification and particle size of eslicarbazepine acetate. The present invention also relates to the physical characteristics of solid state eslicarbazepine acetate, and pharmaceutical compositions containing the same.01-26-2012
20110281928Process for the preparation of zofenopril and its pharmaceutically acceptable salts thereof - The present invention relates to a process for the preparation of zofenopril and its pharmaceutically acceptable salts and a pharmaceutical composition thereof. The present invention also provides structurally novel compounds, which are useful intermediates in the synthesis of zofenopril.11-17-2011
20110207779PROCESS FOR THE PREPARATION OF ESOMEPRAZOLE MAGNESIUM - The present invention relates to a process for the preparation of esomeprazole magnesium containing R-isomer greater than about 0.1% by wt. In particular, the present invention relates to a process for the preparation of esomeprazole magnesium dihydrate containing R-isomer greater than about 0.1% by wt.08-25-2011
20110105619AMORPHOUS BUPROPION HYDROBROMIDE AND PREPARATION THEREOF - The present invention provides an amorphous bupropion hydrobromide and an amorphous bupropion hydrobromide granulates with at least one pharmaceutically acceptable carrier, and a process for its preparation.05-05-2011
20110053898TOPICAL COMPOSITION COMPRISING VITAMIN D ANALOGUE AND CORTICOSTEROIDS - A topical pharmaceutical composition comprising therapeutically effective amounts of vitamin D or vitamin D analogues, corticosteroid and a straight chain C03-03-2011
20110052687EXTENDED RELEASE PHARMACEUTICAL COMPOSITION OF PALIPERIDONE - The present invention provides an extended release tablet of paliperidone, comprising a) a core containing paliperidone and at least one water soluble and/or gellable polymer, b) a coating comprising at least one water insoluble or permeable polymer, and a water soluble and/or gellable polymer and optionally an enteric polymer.03-03-2011
20110038928ORALLY DISINTEGRATING TABLETS OF ZOLMITRIPTAN - The present invention is directed to a novel rapidly dissolvable pharmaceutical composition comprising zolmitriptan or pharmaceutically acceptable salts or esters thereof and least one direct compression filler. The pharmaceutical compositions of the present invention can advantageously be prepared in a solid dosage form, e.g. a tablet, utilizing directly compressible ingredients.02-17-2011
20100317856PROCESS FOR THE PREPARATION OF R-SITAGLIPTIN AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF - The present invention provides processes for the preparation of R-sitagliptin and its pharmaceutically acceptable salts thereof.12-16-2010
20100310870AMORPHOUS BAZEDOXIFENE ACETATE AND PREPARATION THEREOF - The present invention relates to amorphous form of bazedoxifene acetate and a process for the preparation thereof.12-09-2010
20100292267PALONOSETRON FREE BASE AND PROCESS FOR ITS PREPARATION - The present invention provides novel palonosetron free base in an amorphous form and crystalline form-G and processes for their preparation. The present invention also provides a process for the preparation of palonosetron hydrochloride from the novel palonosetron free base in an amorphous form and/or in crystalline form-G.11-18-2010
20100068284Stable Fixed Dose Topical Formulation - The present invention relates to stable fixed dose topical formulations comprising an antiacne agent and an antibiotic, which exhibit storage stability at a temperature of about 40° C. and relative humidity of about 75% for a period of at least 3 months. Particularly, the present invention relates to stable fixed dose topical formulations comprising therapeutically effective amounts of (a) adapalene-containing microspheres and (b) clindamycin, a process for their preparation thereof and their use for the treatment of acne.03-18-2010
20100028425PHARMACEUTICAL COMPOSITION OF ATOVAQUONE - The present invention relates to immediate release pharmaceutical compositions for oral administration comprising micronized atovaquone particles and at least one drug, wherein about 90% of the atovaquone particles have a volume diameter between about 4 μm to about 8 μm; and having a uniform release profile after a storage for at least three months at 40° C. and 75% relative humidity.02-04-2010
20100008988TABLET COMPOSITIONS OF AMINE POLYMERS - The present invention provides pharmaceutical compositions, essentially comprising less than about 95% by weight of an aliphatic amine polymer. The present invention relates to pharmaceutical compositions comprising aliphatic amine polymers of sevelamer hydrochloride, sevelamer carbonate and colesevelam hydrochloride; and methods of preparing pharmaceutical compositions thereof.01-14-2010
20100008986PHARMACEUTICAL COMPOSITIONS COMPRISING SUMATRIPTAN AND NAPROXEN - The present invention relates to the pharmaceutical composition comprising sumatriptan succinate and naproxen sodium, with a proviso that both the active components are in admixture with each other.01-14-2010
20100004338TOPICAL GEL COMPOSITION COMPRISING AZELAIC ACID - The present invention discloses a novel azelaic acid topical pharmaceutical gel composition that does not contain lecithin and a process for its preparation.01-07-2010
20100003319RALOXIFENE IMMEDIATE RELEASE TABLETS - The present invention relates generally to formulations containing raloxifene or pharmaceutical salts thereof, as the active pharmaceutical ingredient and a process for preparing the same.01-07-2010
20090298884Esomeprazole Strontium Salt, Process For Its Preparation and Pharmaceutical Compositions Containing Same - A strontium salt of esomeprazole is provided. A process for preparing a strontium salt of esomeprazole is also provided comprising reacting esomeprazole free base or a sodium, potassium or lithium salt of esomeprazole with a strontium source in one or more solvents.12-03-2009
20090298803PHARMACEUTICAL COMPOSITION COMPRISING FLUOCINONIDE - The present invention provides a composition, comprising fluocinonide in a vehicle comprising one or two penetration enhancers, solvents and emulsifiers wherein penetration enhancers are present in ratio of less than 0.90 to the total of the penetration enhancers, solvents and emulsifiers.12-03-2009

Patent applications by Glenmark Generics Ltd.