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
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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
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)
71335-1866-5 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 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-5)
71335-1866-6 71335-1866 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220906 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1866-6)
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)
68071-2890-3 68071-2890 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221130 N/A ANDA ANDA205794 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-2890-3)
68071-2890-6 68071-2890 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250826 N/A ANDA ANDA205794 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-2890-6)
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)
50090-6871-1 50090-6871 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231204 N/A ANDA ANDA205794 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1)
50090-6872-0 50090-6872 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231204 N/A ANDA ANDA205794 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6872-0)
50090-6871-2 50090-6871 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231204 N/A ANDA ANDA205794 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2)
50090-6871-3 50090-6871 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231204 N/A ANDA ANDA205794 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3)
50090-6871-0 50090-6871 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231204 N/A ANDA ANDA205794 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0)
71335-1984-1 71335-1984 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220127 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-1)
71335-1984-5 71335-1984 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-5)
71335-1984-6 71335-1984 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-6)
71335-1984-2 71335-1984 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-2)
71335-1984-3 71335-1984 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220406 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-3)
71335-1984-4 71335-1984 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA205794 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 200 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-1984-4)
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