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=ANDA211551"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
42571-312-90 42571-312 HUMAN OTC DRUG Levocetirizine Dihydrochloride Levocetirizine Dihydrochloride TABLET ORAL 20190201 N/A ANDA ANDA211551 Micro Labs Limited LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (42571-312-90) / 90 TABLET in 1 BOTTLE
42571-312-53 42571-312 HUMAN OTC DRUG Levocetirizine Dihydrochloride Levocetirizine Dihydrochloride TABLET ORAL 20190201 N/A ANDA ANDA211551 Micro Labs Limited LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 2500 TABLET in 1 POUCH (42571-312-53)
42571-312-18 42571-312 HUMAN OTC DRUG Levocetirizine Dihydrochloride Levocetirizine Dihydrochloride TABLET ORAL 20190201 N/A ANDA ANDA211551 Micro Labs Limited LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 1 BOTTLE in 1 CARTON (42571-312-18) / 10 TABLET in 1 BOTTLE
42571-312-11 42571-312 HUMAN OTC DRUG Levocetirizine Dihydrochloride Levocetirizine Dihydrochloride TABLET ORAL 20190201 N/A ANDA ANDA211551 Micro Labs Limited LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1 100 BLISTER PACK in 1 CARTON (42571-312-11) / 10 TABLET in 1 BLISTER PACK (42571-312-32)
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