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=ANDA211518"
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
72865-118-05 72865-118 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20200217 N/A ANDA ANDA211518 XLCare Pharmaceuticals, Inc. BENZONATATE 150 mg/1 500 CAPSULE in 1 BOTTLE (72865-118-05)
72865-118-30 72865-118 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20200217 N/A ANDA ANDA211518 XLCare Pharmaceuticals, Inc. BENZONATATE 150 mg/1 30 CAPSULE in 1 BOTTLE (72865-118-30)
71205-887-14 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 14 CAPSULE in 1 BOTTLE (71205-887-14)
71205-887-15 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 15 CAPSULE in 1 BOTTLE (71205-887-15)
71205-887-20 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 20 CAPSULE in 1 BOTTLE (71205-887-20)
71205-887-21 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 21 CAPSULE in 1 BOTTLE (71205-887-21)
71205-887-30 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 30 CAPSULE in 1 BOTTLE (71205-887-30)
71205-887-55 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 500 CAPSULE in 1 BOTTLE (71205-887-55)
71205-887-00 71205-887 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210917 N/A ANDA ANDA211518 Proficient Rx LP BENZONATATE 200 mg/1 100 CAPSULE in 1 BOTTLE (71205-887-00)
72865-119-30 72865-119 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20200217 N/A ANDA ANDA211518 XLCare Pharmaceuticals, Inc. BENZONATATE 200 mg/1 30 CAPSULE in 1 BOTTLE (72865-119-30)
31722-958-01 31722-958 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20190222 N/A ANDA ANDA211518 Camber Pharmaceuticals, Inc. BENZONATATE 200 mg/1 100 CAPSULE in 1 BOTTLE (31722-958-01)
31722-958-05 31722-958 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20190222 N/A ANDA ANDA211518 Camber Pharmaceuticals, Inc. BENZONATATE 200 mg/1 500 CAPSULE in 1 BOTTLE (31722-958-05)
31722-958-30 31722-958 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20190222 N/A ANDA ANDA211518 Camber Pharmaceuticals, Inc. BENZONATATE 200 mg/1 30 CAPSULE in 1 BOTTLE (31722-958-30)
67296-1833-3 67296-1833 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20190222 N/A ANDA ANDA211518 Redpharm drug, inc BENZONATATE 200 mg/1 30 CAPSULE in 1 BOTTLE (67296-1833-3)
71335-2486-0 71335-2486 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20240918 N/A ANDA ANDA211518 Bryant Ranch Prepack BENZONATATE 200 mg/1 6 CAPSULE in 1 BOTTLE (71335-2486-0)
71335-2486-1 71335-2486 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20240918 N/A ANDA ANDA211518 Bryant Ranch Prepack BENZONATATE 200 mg/1 30 CAPSULE in 1 BOTTLE (71335-2486-1)
71335-2486-2 71335-2486 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20240918 N/A ANDA ANDA211518 Bryant Ranch Prepack BENZONATATE 200 mg/1 100 CAPSULE in 1 BOTTLE (71335-2486-2)
71335-2486-3 71335-2486 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20240918 N/A ANDA ANDA211518 Bryant Ranch Prepack BENZONATATE 200 mg/1 45 CAPSULE in 1 BOTTLE (71335-2486-3)
71335-2486-4 71335-2486 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20240918 N/A ANDA ANDA211518 Bryant Ranch Prepack BENZONATATE 200 mg/1 20 CAPSULE in 1 BOTTLE (71335-2486-4)
71335-2486-5 71335-2486 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20240918 N/A ANDA ANDA211518 Bryant Ranch Prepack BENZONATATE 200 mg/1 15 CAPSULE in 1 BOTTLE (71335-2486-5)
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