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=NDA018276"
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
67296-0757-2 67296-0757 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 19811016 N/A NDA AUTHORIZED GENERIC NDA018276 RedPharm Drug Inc ALPRAZOLAM .5 mg/1 20 TABLET in 1 BOTTLE (67296-0757-2)
58151-452-01 58151-452 HUMAN PRESCRIPTION DRUG Xanax alprazolam TABLET ORAL 20251029 N/A NDA NDA018276 Viatris Specialty LLC ALPRAZOLAM .25 mg/1 100 TABLET in 1 BOTTLE (58151-452-01)
58151-452-05 58151-452 HUMAN PRESCRIPTION DRUG Xanax alprazolam TABLET ORAL 20251029 N/A NDA NDA018276 Viatris Specialty LLC ALPRAZOLAM .25 mg/1 500 TABLET in 1 BOTTLE (58151-452-05)
58151-453-01 58151-453 HUMAN PRESCRIPTION DRUG Xanax alprazolam TABLET ORAL 20250710 N/A NDA NDA018276 Viatris Specialty LLC ALPRAZOLAM .5 mg/1 100 TABLET in 1 BOTTLE (58151-453-01)
58151-453-05 58151-453 HUMAN PRESCRIPTION DRUG Xanax alprazolam TABLET ORAL 20251002 N/A NDA NDA018276 Viatris Specialty LLC ALPRAZOLAM .5 mg/1 500 TABLET in 1 BOTTLE (58151-453-05)
58151-454-01 58151-454 HUMAN PRESCRIPTION DRUG Xanax alprazolam TABLET ORAL 20251002 N/A NDA NDA018276 Viatris Specialty LLC ALPRAZOLAM 1 mg/1 100 TABLET in 1 BOTTLE (58151-454-01)
58151-455-01 58151-455 HUMAN PRESCRIPTION DRUG Xanax alprazolam TABLET ORAL 20251029 N/A NDA NDA018276 Viatris Specialty LLC ALPRAZOLAM 2 mg/1 100 TABLET in 1 BOTTLE (58151-455-01)
71205-614-02 71205-614 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20211015 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 1 mg/1 2 TABLET in 1 BOTTLE (71205-614-02)
71205-614-30 71205-614 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20211015 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 1 mg/1 30 TABLET in 1 BOTTLE (71205-614-30)
71205-614-60 71205-614 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20211015 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 1 mg/1 60 TABLET in 1 BOTTLE (71205-614-60)
71205-614-90 71205-614 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20211015 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 1 mg/1 90 TABLET in 1 BOTTLE (71205-614-90)
71205-652-30 71205-652 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20220412 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM .5 mg/1 30 TABLET in 1 BOTTLE (71205-652-30)
71205-652-60 71205-652 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20220412 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM .5 mg/1 60 TABLET in 1 BOTTLE (71205-652-60)
71205-652-90 71205-652 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20220412 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM .5 mg/1 90 TABLET in 1 BOTTLE (71205-652-90)
63187-971-30 63187-971 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20180101 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 2 mg/1 30 TABLET in 1 BOTTLE (63187-971-30)
63187-971-60 63187-971 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20180101 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 2 mg/1 60 TABLET in 1 BOTTLE (63187-971-60)
63187-971-90 63187-971 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 20180101 N/A NDA AUTHORIZED GENERIC NDA018276 Proficient Rx LP ALPRAZOLAM 2 mg/1 90 TABLET in 1 BOTTLE (63187-971-90)
59762-3719-1 59762-3719 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 19811016 N/A NDA AUTHORIZED GENERIC NDA018276 Mylan Pharmaceuticals Inc. ALPRAZOLAM .25 mg/1 100 TABLET in 1 BOTTLE (59762-3719-1)
59762-3719-3 59762-3719 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 19811016 N/A NDA AUTHORIZED GENERIC NDA018276 Mylan Pharmaceuticals Inc. ALPRAZOLAM .25 mg/1 500 TABLET in 1 BOTTLE (59762-3719-3)
59762-3719-4 59762-3719 HUMAN PRESCRIPTION DRUG Alprazolam alprazolam TABLET ORAL 19811016 N/A NDA AUTHORIZED GENERIC NDA018276 Mylan Pharmaceuticals Inc. ALPRAZOLAM .25 mg/1 1000 TABLET in 1 BOTTLE (59762-3719-4)
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