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=ANDA205794"
符合检索条件的记录共 99 条，共 5 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
71610-990-53 71610-990 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260227 N/A ANDA ANDA205794 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-990-53)
71610-990-60 71610-990 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260227 N/A ANDA ANDA205794 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-990-60)
71610-582-83 71610-582 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210715 N/A ANDA ANDA205794 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 200 mg/1 3600 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-582-83)
50228-174-01 50228-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-01)
50228-174-05 50228-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-05)
50228-174-10 50228-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-10)
43598-752-01 43598-752 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA205794 Dr. Reddy’s Laboratories Inc. BUPROPION HYDROCHLORIDE 150 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-752-01)
43598-752-05 43598-752 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA205794 Dr. Reddy’s Laboratories Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-752-05)
43598-752-60 43598-752 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA205794 Dr. Reddy’s Laboratories Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-752-60)
50228-174-30 50228-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-30)
50228-174-60 50228-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-174-60)
63629-8473-1 63629-8473 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8473-1)
71335-1866-1 71335-1866 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210621 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-1)
71335-1866-2 71335-1866 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240717 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-2)
71335-1866-3 71335-1866 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210916 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-3)
71335-1866-4 71335-1866 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240717 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-4)
77771-175-05 77771-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210415 N/A ANDA ANDA205794 Radha Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-175-05)
77771-175-60 77771-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210415 N/A ANDA ANDA205794 Radha Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-175-60)
72789-158-60 72789-158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210118 N/A ANDA ANDA205794 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-158-60)
71610-576-30 71610-576 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210811 N/A ANDA ANDA205794 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-576-30)
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