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=NDA021992"
符合检索条件的记录共 12 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0008-1210-30 0008-1210 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20150401 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 25 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1210-30)
0008-1222-01 0008-1222 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1222-01)
0008-1222-14 0008-1222 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 100 mg/1 14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1222-14)
0008-1222-30 0008-1222 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1222-30)
0008-1222-50 0008-1222 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 100 mg/1 100 BLISTER PACK in 1 CARTON (0008-1222-50) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
59762-1211-3 59762-1211 HUMAN PRESCRIPTION DRUG Desvenlafaxine Succinate desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20170301 N/A NDA AUTHORIZED GENERIC NDA021992 Greenstone LLC DESVENLAFAXINE SUCCINATE 50 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59762-1211-3)
0008-1211-01 0008-1211 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 50 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1211-01)
0008-1211-14 0008-1211 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 50 mg/1 14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1211-14)
0008-1211-30 0008-1211 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 50 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1211-30)
0008-1211-50 0008-1211 HUMAN PRESCRIPTION DRUG Pristiq Extended-Release desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20080501 N/A NDA NDA021992 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. DESVENLAFAXINE SUCCINATE 50 mg/1 100 BLISTER PACK in 1 CARTON (0008-1211-50) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
59762-1210-3 59762-1210 HUMAN PRESCRIPTION DRUG Desvenlafaxine Succinate desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20170301 N/A NDA AUTHORIZED GENERIC NDA021992 Greenstone LLC DESVENLAFAXINE SUCCINATE 25 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59762-1210-3)
59762-1222-3 59762-1222 HUMAN PRESCRIPTION DRUG Desvenlafaxine Succinate desvenlafaxine succinate TABLET, EXTENDED RELEASE ORAL 20170301 N/A NDA AUTHORIZED GENERIC NDA021992 Greenstone LLC DESVENLAFAXINE SUCCINATE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59762-1222-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2023 Drugfuture->U.S. FDA National Drug Code DataBase