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 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
60505-0158-3 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)
60505-0158-5 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)
60505-0158-7 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)
60505-0158-9 60505-0158 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)
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)
45865-473-30 45865-473 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20210908 N/A ANDA ANDA076143 Medsource Pharmaceuticals BUPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (45865-473-30)
68001-308-00 68001-308 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20170208 N/A ANDA ANDA076143 BluePoint Laboratories BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68001-308-00)
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)
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)
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)
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
70518-1584-0 70518-1584 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20181024 N/A ANDA ANDA076143 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1584-0)
70518-1584-1 70518-1584 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20190219 N/A ANDA ANDA076143 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1584-1)
60505-0157-1 60505-0157 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0157-1)
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