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=ANDA074342"
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
50090-5078-0 50090-5078 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20200617 N/A ANDA ANDA074342 A-S Medication Solutions ALPRAZOLAM .5 mg/1 30 TABLET in 1 BOTTLE (50090-5078-0)
50090-5078-2 50090-5078 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20230918 N/A ANDA ANDA074342 A-S Medication Solutions ALPRAZOLAM .5 mg/1 60 TABLET in 1 BOTTLE (50090-5078-2)
50090-5078-3 50090-5078 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20200617 N/A ANDA ANDA074342 A-S Medication Solutions ALPRAZOLAM .5 mg/1 90 TABLET in 1 BOTTLE (50090-5078-3)
0228-2031-10 0228-2031 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Actavis Pharma, Inc. ALPRAZOLAM 1 mg/1 100 TABLET in 1 BOTTLE (0228-2031-10)
0228-2031-50 0228-2031 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Actavis Pharma, Inc. ALPRAZOLAM 1 mg/1 500 TABLET in 1 BOTTLE (0228-2031-50)
0228-2031-96 0228-2031 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Actavis Pharma, Inc. ALPRAZOLAM 1 mg/1 1000 TABLET in 1 BOTTLE (0228-2031-96)
80425-0099-2 80425-0099 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Advanced Rx of Tennessee, LLC ALPRAZOLAM .5 mg/1 60 TABLET in 1 BOTTLE (80425-0099-2)
68071-2292-1 68071-2292 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20201116 N/A ANDA ANDA074342 NuCare Pharmaceuticals,Inc. ALPRAZOLAM .25 mg/1 10 TABLET in 1 BOTTLE (68071-2292-1)
0228-2027-10 0228-2027 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Actavis Pharma, Inc. ALPRAZOLAM .25 mg/1 100 TABLET in 1 BOTTLE (0228-2027-10)
0228-2027-50 0228-2027 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Actavis Pharma, Inc. ALPRAZOLAM .25 mg/1 500 TABLET in 1 BOTTLE (0228-2027-50)
0228-2027-96 0228-2027 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 19931001 N/A ANDA ANDA074342 Actavis Pharma, Inc. ALPRAZOLAM .25 mg/1 1000 TABLET in 1 BOTTLE (0228-2027-96)
83008-010-30 83008-010 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20230307 20260831 ANDA ANDA074342 Quality Care Products, LLC ALPRAZOLAM 1 mg/1 30 TABLET in 1 BOTTLE (83008-010-30)
68071-2220-3 68071-2220 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20200721 N/A ANDA ANDA074342 NuCare Pharmaceuticals,Inc. ALPRAZOLAM .5 mg/1 30 TABLET in 1 BOTTLE (68071-2220-3)
71335-0849-0 71335-0849 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20220502 N/A ANDA ANDA074342 Bryant Ranch Prepack ALPRAZOLAM .5 mg/1 10 TABLET in 1 BOTTLE (71335-0849-0)
71335-0849-1 71335-0849 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20180620 N/A ANDA ANDA074342 Bryant Ranch Prepack ALPRAZOLAM .5 mg/1 15 TABLET in 1 BOTTLE (71335-0849-1)
71335-0849-2 71335-0849 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20180608 N/A ANDA ANDA074342 Bryant Ranch Prepack ALPRAZOLAM .5 mg/1 30 TABLET in 1 BOTTLE (71335-0849-2)
71335-0849-3 71335-0849 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20220502 N/A ANDA ANDA074342 Bryant Ranch Prepack ALPRAZOLAM .5 mg/1 20 TABLET in 1 BOTTLE (71335-0849-3)
71335-0849-4 71335-0849 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20220502 N/A ANDA ANDA074342 Bryant Ranch Prepack ALPRAZOLAM .5 mg/1 100 TABLET in 1 BOTTLE (71335-0849-4)
71335-0849-5 71335-0849 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20180906 N/A ANDA ANDA074342 Bryant Ranch Prepack ALPRAZOLAM .5 mg/1 90 TABLET in 1 BOTTLE (71335-0849-5)
71610-112-30 71610-112 HUMAN PRESCRIPTION DRUG Alprazolam Alprazolam TABLET ORAL 20180806 N/A ANDA ANDA074342 Aphena Pharma Solutions - Tennessee, LLC ALPRAZOLAM .25 mg/1 30 TABLET in 1 BOTTLE (71610-112-30)
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