PROCESS FOR PREPARING PHARMACEUTICAL OPHTHALMIC COMPOSITIONS
    3.
    发明公开
    PROCESS FOR PREPARING PHARMACEUTICAL OPHTHALMIC COMPOSITIONS 审中-公开
    程序对药物组合物对于眼睛的制备

    公开(公告)号:EP2506878A2

    公开(公告)日:2012-10-10

    申请号:EP10801718.7

    申请日:2010-12-02

    申请人: Lupin Limited

    摘要: Pharmaceutical ophthalmic compositions comprising active ingredient(s) such as carbonic anhydrase inhibitor (CAI) or combinations and processes for making such compositions and the use of these compositions in patient populations including pediatric populations. A process for preparing an ophthalmic composition comprising a carbonic anhydrase inhibitor, which comprises a) preparing a slurry comprising a carbonic anhydrase inhibitor and a surfactant; b) preparing a polymer slurry comprising a polymer and water; c) preparing a solution comprising tonicity and preservative agents; d) mixing the polymer slurry of step b and the solution of step c, to form a vehicle concentrate and adjusting pH; e) adding the slurry of step a, to the vehicle concentrate of step d and mixing to homogenize; f) autoclaving the mixture of step e; g) sizing the mixture of step f, under aseptic condition.

    摘要翻译: 药物组合物包括眼用活性成分:如碳酸酐酶抑制剂(CAI)或其组合以及制造的搜索的组合物和在患者人群包括儿童群体使用合成的组合物的过程。 一种用于制备表面活性剂的眼用组合物,包含碳酸酐酶抑制剂,其包括a)制备浆液,其包含碳酸酐酶抑制剂和的方法; b)制备的聚合物淤浆,其包括聚合物和水; c)制备的溶液,其包括张力剂和防腐剂; d)将步骤b的聚合物淤浆和步骤c的所述溶液,以形成车辆浓缩物和调节pH值; e)加入步骤a的浆料,步骤d的车辆浓缩物和混合以匀化; F)热压工序e的混合物; 克)施胶步骤f的混合物中,无菌条件下。

    BILAYER TABLET OF DRONEDARONE
    4.
    发明公开
    BILAYER TABLET OF DRONEDARONE 审中-公开
    DOPPELSCHICHTTABLETTE AUS DRONEDARON

    公开(公告)号:EP2817001A1

    公开(公告)日:2014-12-31

    申请号:EP13708528.8

    申请日:2013-02-14

    申请人: Lupin Limited

    IPC分类号: A61K9/24 A61K31/343

    CPC分类号: A61K31/343 A61K9/209

    摘要: The present invention relates to multi component composition of dronedarone or pharmaceutically acceptable salts, esters, metabolites, prodrugs or enantiomers thereof and controlled release polymers. The use of multi component composition of Dronedarone would improve the bioavailability and the patient compliance with reduction in number of dosages to be taken per day.

    摘要翻译: 本发明涉及决奈达隆或其药学上可接受的盐,酯,代谢物,前药或对映异构体和控释聚合物的多组分组合物。 使用多组分组合物的决奈达隆将提高生物利用度和患者依从性,减少每日服用的剂量。

    SUSTAINED RELEASE COMPOSITION OF MEMANTINE
    7.
    发明公开
    SUSTAINED RELEASE COMPOSITION OF MEMANTINE 审中-公开
    RETARD-ZUSAMMENSETZUNG AUS MEMANTIN

    公开(公告)号:EP2675435A1

    公开(公告)日:2013-12-25

    申请号:EP12706927.6

    申请日:2012-02-07

    申请人: Lupin Limited

    IPC分类号: A61K9/16 A61K9/50 A61K31/13

    摘要: A sustained release pharmaceutical composition comprising; a core including memantine or its pharmaceutically acceptable salts and one or more pharmaceutical acceptable excipients, and a sustained release coating comprising a water insoluble substance and a water soluble substance where the ratio of the water insoluble substance to the water soluble substance is from about 1:0 to about 3:5:1, optionally containing an immediate release coating having memantine where the immediate release coating is applied over the sustained release coating.

    摘要翻译: 一种缓释药物组合物,其包含: 包括美金刚或其药学上可接受的盐和一种或多种药学上可接受的赋形剂的核心,以及包含水不溶性物质和水溶性物质的持续释放包衣,其中水不溶性物质与水溶性物质的比例为约1: 0至约3:5:1,任选地包含具有美金刚的速释涂层,其中速释涂层施用于缓释涂层上。