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"
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
68788-7988-6 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)
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)
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)
72162-2098-1 72162-2098 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2098-1)
55154-8180-0 55154-8180 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180129 N/A ANDA ANDA076143 Cardinal Health 107, LLC BUPROPION HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 BAG (55154-8180-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68071-2256-1 68071-2256 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20200910 N/A ANDA ANDA076143 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68071-2256-1)
70518-1566-0 70518-1566 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20181222 N/A ANDA ANDA076143 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)
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)
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)
71335-0182-7 71335-0182 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210428 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)
71335-0013-5 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)
71335-0013-6 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)
71335-0013-7 71335-0013 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240709 N/A ANDA ANDA076143 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)
82804-123-30 82804-123 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA076143 Proficient Rx LP BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-123-30)
71610-164-83 71610-164 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180926 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 100 mg/1 3600 TABLET, FILM COATED in 1 BOTTLE (71610-164-83)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase