美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）
检索条件:" 注册申请号=ANDA210375"
符合检索条件的记录共 44 条，共 3 页，当前第 3 页 ，可点击列名称排序
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NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
11673-847-16 11673-847 HUMAN OTC DRUG levocetirizine dihydrochloride levocetirizine dihydrochloride TABLET, COATED ORAL 20201201 N/A ANDA ANDA210375 Target Corporation LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 2 BOTTLE in 1 CARTON (11673-847-16) / 80 TABLET, COATED in 1 BOTTLE
11673-847-35 11673-847 HUMAN OTC DRUG levocetirizine dihydrochloride levocetirizine dihydrochloride TABLET, COATED ORAL 20181231 N/A ANDA ANDA210375 Target Corporation LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (11673-847-35) / 35 TABLET, COATED in 1 BOTTLE
11673-847-80 11673-847 HUMAN OTC DRUG levocetirizine dihydrochloride levocetirizine dihydrochloride TABLET, COATED ORAL 20181231 N/A ANDA ANDA210375 Target Corporation LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (11673-847-80) / 80 TABLET, COATED in 1 BOTTLE
41163-938-35 41163-938 HUMAN OTC DRUG levocetirizine dihydrochloride levocetirizine dihydrochloride TABLET, COATED ORAL 20181231 N/A ANDA ANDA210375 United Natural Foods, Inc. dba UNFI LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (41163-938-35) / 35 TABLET, COATED in 1 BOTTLE
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