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=ANDA078203"
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
68071-3242-4 68071-3242 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20170523 N/A ANDA ANDA078203 NuCare Pharmaceuticals, Inc. LORAZEPAM 1 mg/1 4 TABLET in 1 BOTTLE (68071-3242-4)
68071-3242-5 68071-3242 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20170523 N/A ANDA ANDA078203 NuCare Pharmaceuticals, Inc. LORAZEPAM 1 mg/1 15 TABLET in 1 BOTTLE (68071-3242-5)
68071-3242-6 68071-3242 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20170523 N/A ANDA ANDA078203 NuCare Pharmaceuticals, Inc. LORAZEPAM 1 mg/1 6 TABLET in 1 BOTTLE (68071-3242-6)
68071-3242-8 68071-3242 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20170523 N/A ANDA ANDA078203 NuCare Pharmaceuticals, Inc. LORAZEPAM 1 mg/1 8 TABLET in 1 BOTTLE (68071-3242-8)
69315-906-01 69315-906 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230516 N/A ANDA ANDA078203 Leading Pharma, LLC LORAZEPAM 2 mg/1 100 TABLET in 1 BOTTLE (69315-906-01)
69315-906-05 69315-906 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230516 N/A ANDA ANDA078203 Leading Pharma, LLC LORAZEPAM 2 mg/1 500 TABLET in 1 BOTTLE (69315-906-05)
69315-906-10 69315-906 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230516 N/A ANDA ANDA078203 Leading Pharma, LLC LORAZEPAM 2 mg/1 1000 TABLET in 1 BOTTLE (69315-906-10)
70518-1520-0 70518-1520 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20181011 N/A ANDA ANDA078203 REMEDYREPACK INC. LORAZEPAM .5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1520-0)
70518-1520-1 70518-1520 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20210810 N/A ANDA ANDA078203 REMEDYREPACK INC. LORAZEPAM .5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1520-1)
71335-1467-0 71335-1467 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20240403 N/A ANDA ANDA078203 Bryant Ranch Prepack LORAZEPAM 1 mg/1 10 TABLET in 1 BOTTLE (71335-1467-0)
71610-255-28 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20231130 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 28 TABLET in 1 BOTTLE (71610-255-28)
71610-255-30 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 30 TABLET in 1 BOTTLE (71610-255-30)
71610-255-45 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 45 TABLET in 1 BOTTLE (71610-255-45)
71610-255-53 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 60 TABLET in 1 BOTTLE (71610-255-53)
71610-255-55 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 75 TABLET in 1 BOTTLE (71610-255-55)
71610-255-60 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 90 TABLET in 1 BOTTLE (71610-255-60)
71610-255-70 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 120 TABLET in 1 BOTTLE (71610-255-70)
71610-255-75 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20240115 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 150 TABLET in 1 BOTTLE (71610-255-75)
71610-255-80 71610-255 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20230830 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 1 mg/1 180 TABLET in 1 BOTTLE (71610-255-80)
71610-178-60 71610-178 HUMAN PRESCRIPTION DRUG Lorazepam Lorazepam TABLET ORAL 20181024 N/A ANDA ANDA078203 Aphena Pharma Solutions - Tennessee, LLC LORAZEPAM 2 mg/1 90 TABLET in 1 BOTTLE (71610-178-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase