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 95 条，共 5 页，当前第 3 页 ，可点击列名称排序
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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
43598-537-05 43598-537 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160801 N/A ANDA ANDA205794 Dr. Reddy’s Laboratories Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-537-05)
43598-537-60 43598-537 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160801 N/A ANDA ANDA205794 Dr. Reddy’s Laboratories Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-537-60)
43598-538-60 43598-538 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20160801 N/A ANDA ANDA205794 Dr. Reddy’s Laboratories Inc. BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-538-60)
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)
82868-019-30 82868-019 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240314 N/A ANDA ANDA205794 Northwind Health Company, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-30)
82868-019-60 82868-019 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231019 N/A ANDA ANDA205794 Northwind Health Company, LLC BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-60)
82868-019-90 82868-019 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250102 N/A ANDA ANDA205794 Northwind Health Company, LLC BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-90)
82868-019-96 82868-019 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240219 N/A ANDA ANDA205794 Northwind Health Company, LLC BUPROPION HYDROCHLORIDE 150 mg/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-019-96)
70518-4056-1 70518-4056 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250123 N/A ANDA ANDA205794 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4056-1)
43598-751-01 43598-751 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 100 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-751-01)
43598-751-05 43598-751 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 100 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-751-05)
43598-751-60 43598-751 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 100 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-751-60)
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)
43598-753-60 43598-753 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 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-753-60)
68788-7793-1 68788-7793 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201013 N/A ANDA ANDA205794 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-1)
68788-7793-2 68788-7793 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201013 N/A ANDA ANDA205794 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-2)
68788-7793-3 68788-7793 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201013 N/A ANDA ANDA205794 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-3)
68788-7793-6 68788-7793 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201013 N/A ANDA ANDA205794 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-6)
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