Pharmaceutical formulation of cefixime for enhanced bioavailability
    1.
    发明授权
    Pharmaceutical formulation of cefixime for enhanced bioavailability 有权
    头孢克肟的药物制剂,以提高生物利用度

    公开(公告)号:US09149482B2

    公开(公告)日:2015-10-06

    申请号:US11579988

    申请日:2004-05-10

    CPC分类号: A61K31/546 A61K9/0056

    摘要: A chewable tablet comprising Cefixime having a mean particle size between 20μ and 120μ wherein the said composition demonstrates bioequivalence to a suspension of Cefixime trihydrate. The process of preparation of the chewable tablet comprises the steps of optionally micronizing Cefixime such that the mean particle size of the Cefixime particles is between 20μ and 120μ, blending with other excipients, roll compaction, milling to form granules, blending to form a secondary blend and compression of the secondary blend to form tablets.

    摘要翻译: 一种咀嚼片,其包含平均粒径在20μ和120μ之间的头孢克肟,其中所述组合物显示与头孢克肟三水合物的悬浮液的生物等效性。 咀嚼片的制备方法包括以下步骤:任选地将头孢克肟微粉化,使得头孢克肟颗粒的平均粒径为20-120μ,与其它赋形剂混合,辊压,研磨形成颗粒,共混以形成二次共混物 并压制二次共混物以形成片剂。

    Novel Pharmaceutical Formulation of Cefixime for Enhanced Bioavailability
    4.
    发明申请
    Novel Pharmaceutical Formulation of Cefixime for Enhanced Bioavailability 有权
    头孢克肟的新型药物制剂用于提高生物利用度

    公开(公告)号:US20070286901A1

    公开(公告)日:2007-12-13

    申请号:US11579988

    申请日:2004-05-10

    IPC分类号: A61K9/20 A61K31/545 A61P31/04

    CPC分类号: A61K31/546 A61K9/0056

    摘要: A chewable tablet comprising Cefixime having a mean particle size between 20 μ and 120 μ wherein the said composition demonstrates bioequivalence to a suspension of Cefixime trihydrate. The process of preparation of the chewable tablet comprises the steps of optionally micronizing Cefixime such that the mean particle size of the Cefixime particles is between 20 μ and 120 μ, blending with other excipients, roll compaction, milling to form granules, blending to form a secondary blend and compression of the secondary blend to form tablets.

    摘要翻译: 一种包含Cefixime的咀嚼片,其平均粒度为20-120微米,其中所述组合物显示出Cefixime三水合物的悬浮液的生物等效性。 咀嚼片的制备方法包括以下步骤:任选地将头孢克肟微粉化,使得头孢克肟颗粒的平均粒度为20-120微米,与其它赋形剂混合,辊压,研磨形成颗粒,混合形成 二次混合和二次混合物的压缩以形成片剂。