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=NDA017892"
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
43353-451-30 43353-451 HUMAN PRESCRIPTION DRUG Triazolam triazolam TABLET ORAL 19821115 N/A NDA AUTHORIZED GENERIC NDA017892 Aphena Pharma Solutions - Tennessee, LLC TRIAZOLAM .25 mg/1 30 TABLET in 1 BOTTLE (43353-451-30)
43353-451-53 43353-451 HUMAN PRESCRIPTION DRUG Triazolam triazolam TABLET ORAL 19821115 N/A NDA AUTHORIZED GENERIC NDA017892 Aphena Pharma Solutions - Tennessee, LLC TRIAZOLAM .25 mg/1 60 TABLET in 1 BOTTLE (43353-451-53)
59762-3717-9 59762-3717 HUMAN PRESCRIPTION DRUG Triazolam triazolam TABLET ORAL 20170113 N/A NDA AUTHORIZED GENERIC NDA017892 Greenstone LLC TRIAZOLAM .125 mg/1 100 TABLET in 1 BOTTLE (59762-3717-9)
59762-3718-3 59762-3718 HUMAN PRESCRIPTION DRUG Triazolam triazolam TABLET ORAL 19821115 N/A NDA AUTHORIZED GENERIC NDA017892 Greenstone LLC TRIAZOLAM .25 mg/1 500 TABLET in 1 BOTTLE (59762-3718-3)
59762-3718-9 59762-3718 HUMAN PRESCRIPTION DRUG Triazolam triazolam TABLET ORAL 20170113 N/A NDA AUTHORIZED GENERIC NDA017892 Greenstone LLC TRIAZOLAM .25 mg/1 100 TABLET in 1 BOTTLE (59762-3718-9)
0009-0017-55 0009-0017 HUMAN PRESCRIPTION DRUG Halcion triazolam TABLET ORAL 19821115 20260630 NDA NDA017892 Pharmacia & Upjohn Company LLC TRIAZOLAM .25 mg/1 100 BLISTER PACK in 1 CARTON (0009-0017-55) / 1 TABLET in 1 BLISTER PACK
0009-0017-58 0009-0017 HUMAN PRESCRIPTION DRUG Halcion triazolam TABLET ORAL 19821115 N/A NDA NDA017892 Pharmacia & Upjohn Company LLC TRIAZOLAM .25 mg/1 10 TABLET in 1 BOTTLE (0009-0017-58)
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