XLS《Sheet1》

"安徽省药品监督抽验不符合标准规定的药品名单" "药品名称","被抽样单位","批号","规格","检验依据","不符合标准规定项目","标示生产单位","检验机构","检验目的","备注" "注射用头孢呋辛钠","铜陵市立医院","160103","1.

25g(按C16H16N4O8S计)","《中国药典》2015年版二部","【检查】溶液的颜色","海南灵康制药有限公司","铜陵市食品药品检验中心","监督抽验-流通环节" "硫酸阿米卡星注射液","铜陵市立医院","1502031","2ml:0.2g(20万单位)","《中国药典》2010年版二部","【检查】可见异物","天津药业集团新郑股份有限公司","铜陵市食品药品检验中心","监督抽验-流通环节" "咽炎片","田家庵区舜济药房","15100100","每片重0.25克","卫生部药品标准中药成方制剂第二册","【性状】","哈尔滨三乐生物工程有限公司","淮南市食品药品检验中心","监督抽验-流通环节" "盐酸黄酮哌酯片","明光市明光街道戴湾村南郢联合医疗室","20160303","0.1g","《中国药典》2015年版二部","【性状】、【检查】溶出度","吉林金恒制药股份有限公司","铜陵市食品药品检验中心","基本药物和高风险药品专项抽验","留样监督抽验合格" "藿香正气水","淮南恒康医药有限公司","20150710","每支装10ml","《中国药典》2010年版一部","【检查】装量","吉林隆泰制药股份有限公司","淮北市食品药品检验中心","基本药物和高风险药品专项抽验", "藿香正气水","淮南三和世纪医药有限公司","20150698","每支装10ml","《中国药典》2010年版一部","【检查】装量","吉林隆泰制药股份有限公司","淮北市食品药品检验中心","基本药物和高风险药品专项抽验", "藿香正气水","安徽永和药业有限公司","20150731","每支装10ml","《中国药典》2010年版一部","【检查】装量","吉林隆泰制药股份有限公司","淮北市食品药品检验中心","基本药物和高风险药品专项抽验", "藿香正气水","安徽金岭药业有限公司","20150601","每支装10ml","《中国药典》2010年版一部","【检查】装量、【含量测定】","湖南马王堆制药有限公司","淮北市食品药品检验中心","基本药物和高风险药品专项抽验" "黄连上清片","绩溪县临溪镇卫生院","150225","每片重0.3克(薄膜衣片)","《中国药典》2010年版一部","【检查】重量差异","上海海虹实业(集团)巢湖今辰药业有限公司","宣城市食品药品检验中心","监督抽验-流通环节","留样监督抽验合格" "说明:

1、性状项是指药品的外观、臭、味、溶解度及物理常数等,外观是对药品的色泽和外表感官的规定.物理常数包括相对密度、馏程、熔点、沸点、比旋度、折光率、黏度、吸收系数等.

2、检查项"可见异物"是指存在于注射剂、眼用液体制剂和无菌原料药中,在规定条件下目视可以观测到的不溶性物质,其粒径或长度通常大于50um;

"溶出度"是指活性药物从片剂、胶囊剂或颗粒剂等制剂在规定条件下溶出的速率和程度.

3、含量测定项是指用化学、仪器或生物测定的方法,对原料及制剂中有效成分的含量进行测定. ,"宣城市食品药品检验所","安神胶囊","100907","部分检验",,