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
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)
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)
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)
77771-174-05 77771-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210415 N/A ANDA ANDA205794 Radha Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-174-05)
77771-174-60 77771-174 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210415 N/A ANDA ANDA205794 Radha Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-174-60)
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)
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)
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)
50090-6871-2 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)
77771-176-60 77771-176 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20210415 N/A ANDA ANDA205794 Radha Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-176-60)
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)
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