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=ANDA076143"
符合检索条件的记录共 65 条，共 4 页，当前第 2 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
68001-309-00 68001-309 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170208 N/A ANDA ANDA076143 BluePoint Laboratories BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68001-309-00)
50268-143-15 50268-143 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170802 N/A ANDA ANDA076143 AvPAK BUPROPION HYDROCHLORIDE 100 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-143-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-143-11)
68788-7988-1 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240311 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7988-1)
68788-7988-3 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7988-3)
68788-7988-6 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7988-6)
68788-7988-9 68788-7988 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210806 N/A ANDA ANDA076143 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7988-9)
72162-2097-1 72162-2097 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2097-1)
82804-127-30 82804-127 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA076143 Proficient Rx LP BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-127-30)
71335-0182-1 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180724 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1)
71335-0182-2 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180620 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2)
71335-0182-3 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)
71335-0182-4 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180328 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)
72789-070-30 72789-070 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20200326 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
72789-070-90 72789-070 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240607 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)
71335-0182-5 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)
71335-0182-6 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)
50268-142-15 50268-142 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170802 N/A ANDA ANDA076143 AvPAK BUPROPION HYDROCHLORIDE 75 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-142-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-142-11)
43063-880-30 43063-880 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180813 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30)
43063-880-60 43063-880 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20181030 N/A ANDA ANDA076143 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 75 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60)
71610-708-80 71610-708 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20230516 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-708-80)
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