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=ANDA210722"
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
71335-2431-3 71335-2431 HUMAN PRESCRIPTION DRUG Loratadine Loratadine TABLET ORAL 20240709 N/A ANDA ANDA210722 Bryant Ranch Prepack LORATADINE 10 mg/1 60 TABLET in 1 BOTTLE (71335-2431-3)
71335-2431-4 71335-2431 HUMAN PRESCRIPTION DRUG Loratadine Loratadine TABLET ORAL 20240709 N/A ANDA ANDA210722 Bryant Ranch Prepack LORATADINE 10 mg/1 14 TABLET in 1 BOTTLE (71335-2431-4)
71335-2431-5 71335-2431 HUMAN PRESCRIPTION DRUG Loratadine Loratadine TABLET ORAL 20240709 N/A ANDA ANDA210722 Bryant Ranch Prepack LORATADINE 10 mg/1 10 TABLET in 1 BOTTLE (71335-2431-5)
71335-2431-6 71335-2431 HUMAN PRESCRIPTION DRUG Loratadine Loratadine TABLET ORAL 20240709 N/A ANDA ANDA210722 Bryant Ranch Prepack LORATADINE 10 mg/1 90 TABLET in 1 BOTTLE (71335-2431-6)
71335-2431-7 71335-2431 HUMAN PRESCRIPTION DRUG Loratadine Loratadine TABLET ORAL 20240709 N/A ANDA ANDA210722 Bryant Ranch Prepack LORATADINE 10 mg/1 28 TABLET in 1 BOTTLE (71335-2431-7)
63654-415-10 63654-415 HUMAN OTC DRUG XL - 3 Allergy XL - 3 Allergy TABLET ORAL 20240410 N/A ANDA ANDA210722 Selder, S.A. de C.V. LORATADINE 10 mg/1 1 BLISTER PACK in 1 CARTON (63654-415-10) / 10 TABLET in 1 BLISTER PACK
80513-711-01 80513-711 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20240101 N/A ANDA ANDA210722 Advanced Rx LLC LORATADINE 10 mg/1 100 TABLET in 1 BOTTLE (80513-711-01)
80513-711-03 80513-711 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20240807 N/A ANDA ANDA210722 Advanced Rx LLC LORATADINE 10 mg/1 300 TABLET in 1 BOTTLE (80513-711-03)
68071-2971-3 68071-2971 HUMAN OTC DRUG LORATADINE LORATADINE TABLET ORAL 20230417 N/A ANDA ANDA210722 NuCare Pharmaceuticals,Inc. LORATADINE 10 mg/1 30 TABLET in 1 BOTTLE (68071-2971-3)
68071-2971-9 68071-2971 HUMAN OTC DRUG LORATADINE LORATADINE TABLET ORAL 20230417 N/A ANDA ANDA210722 NuCare Pharmaceuticals,Inc. LORATADINE 10 mg/1 90 TABLET in 1 BOTTLE (68071-2971-9)
70010-162-01 70010-162 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20211117 N/A ANDA ANDA210722 Granules Pharmaceuticals Inc. LORATADINE 10 mg/1 100 TABLET in 1 BOTTLE (70010-162-01)
70010-162-34 70010-162 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20220501 N/A ANDA ANDA210722 Granules Pharmaceuticals Inc. LORATADINE 10 mg/1 300 TABLET in 1 BOTTLE (70010-162-34)
68998-414-82 68998-414 HUMAN OTC DRUG Allergy Relief Loratadine TABLET ORAL 20220816 N/A ANDA ANDA210722 Marc Glassman, Inc. LORATADINE 10 mg/1 90 TABLET in 1 BOTTLE (68998-414-82)
68998-414-85 68998-414 HUMAN OTC DRUG Allergy Relief Loratadine TABLET ORAL 20200501 N/A ANDA ANDA210722 Marc Glassman, Inc. LORATADINE 10 mg/1 30 TABLET in 1 CARTON (68998-414-85)
62207-787-51 62207-787 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20200101 N/A ANDA ANDA210722 Granules India Ltd LORATADINE 10 mg/1 10 TABLET in 1 BOTTLE (62207-787-51)
62207-787-59 62207-787 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20200101 N/A ANDA ANDA210722 Granules India Ltd LORATADINE 10 mg/1 12 BLISTER PACK in 1 CARTON (62207-787-59) / 10 TABLET in 1 BLISTER PACK
68788-8659-0 68788-8659 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20240513 N/A ANDA ANDA210722 Preferred Pharmaceuticals Inc. LORATADINE 10 mg/1 10 TABLET in 1 BOTTLE (68788-8659-0)
68788-8659-1 68788-8659 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20240513 N/A ANDA ANDA210722 Preferred Pharmaceuticals Inc. LORATADINE 10 mg/1 14 TABLET in 1 BOTTLE (68788-8659-1)
69230-328-01 69230-328 HUMAN OTC DRUG LORATADINE LORATADINE TABLET ORAL 20220731 N/A ANDA ANDA210722 Camber Consumer Care Inc LORATADINE 10 mg/1 1 BOTTLE in 1 CARTON (69230-328-01) / 100 TABLET in 1 BOTTLE
69230-328-03 69230-328 HUMAN OTC DRUG LORATADINE LORATADINE TABLET ORAL 20220731 N/A ANDA ANDA210722 Camber Consumer Care Inc LORATADINE 10 mg/1 300 TABLET in 1 BOTTLE (69230-328-03)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase