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=ANDA219223"
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
25000-092-03 25000-092 HUMAN OTC DRUG Loratadine 10mg Loratadine 10mg TABLET ORAL 20241121 N/A ANDA ANDA219223 MARKSANS PHARMA LIMITED LORATADINE 10 mg/1 1 BOTTLE in 1 CARTON (25000-092-03) / 30 TABLET in 1 BOTTLE
25000-092-79 25000-092 HUMAN OTC DRUG Loratadine 10mg Loratadine 10mg TABLET ORAL 20241121 N/A ANDA ANDA219223 MARKSANS PHARMA LIMITED LORATADINE 10 mg/1 1 BOTTLE in 1 CARTON (25000-092-79) / 150 TABLET in 1 BOTTLE
25000-092-80 25000-092 HUMAN OTC DRUG Loratadine 10mg Loratadine 10mg TABLET ORAL 20241121 N/A ANDA ANDA219223 MARKSANS PHARMA LIMITED LORATADINE 10 mg/1 365 TABLET in 1 BOTTLE (25000-092-80)
25000-092-81 25000-092 HUMAN OTC DRUG Loratadine 10mg Loratadine 10mg TABLET ORAL 20241121 N/A ANDA ANDA219223 MARKSANS PHARMA LIMITED LORATADINE 10 mg/1 2 BLISTER PACK in 1 CARTON (25000-092-81) / 7 TABLET in 1 BLISTER PACK
49483-732-65 49483-732 HUMAN OTC DRUG Loratadine 10 mg Loratadine Tablets USP, 10 mg TABLET ORAL 20250125 N/A ANDA ANDA219223 TIME CAP LABORATORIES, INC. LORATADINE 10 mg/1 365 TABLET in 1 BOTTLE (49483-732-65)
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