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"
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
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)
68788-7793-8 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/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-8)
68788-7793-9 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 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-9)
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)
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)
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)
71610-990-30 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-990-30)
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)
71610-990-80 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/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-990-80)
68788-7807-2 68788-7807 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20201028 N/A ANDA ANDA205794 Preferred Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-2)
72189-349-60 72189-349 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE SR BUPROPION HYDROCHLORIDE SR TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220422 N/A ANDA ANDA205794 DirectRx BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-60)
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)
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)
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