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 4 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
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)
68788-7807-1 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/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-1)
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)
68788-7807-3 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-3)
68788-7807-6 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 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-6)
68788-7807-8 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/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-8)
68788-7807-9 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 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-9)
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)
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)
50228-175-60 50228-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-60)
50228-175-01 50228-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-01)
50228-175-05 50228-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-05)
50228-175-10 50228-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-10)
50228-175-30 50228-175 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-175-30)
50228-176-01 50228-176 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-01)
50228-176-10 50228-176 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180420 N/A ANDA ANDA205794 ScieGen Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-10)
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