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
60687-351-01 60687-351 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180201 N/A ANDA ANDA076143 American Health Packaging BUPROPION HYDROCHLORIDE 100 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-351-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-351-11)
60760-781-30 60760-781 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20250521 N/A ANDA ANDA076143 ST. MARY'S MEDICAL PARK PHARMACY BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)
0904-6636-61 0904-6636 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 100 mg/1 100 BLISTER PACK in 1 CARTON (0904-6636-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60505-0157-5 60505-0157 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Apotex Corp BUPROPION HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (60505-0157-5)
60505-0157-7 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 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0157-7)
60505-0157-9 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 90 TABLET, FILM COATED in 1 BOTTLE (60505-0157-9)
71610-774-53 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240122 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53)
71610-774-70 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240125 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70)
71610-774-80 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240125 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80)
71610-774-94 71610-774 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20240125 N/A ANDA ANDA076143 Aphena Pharma Solutions - Tennessee, LLC BUPROPION HYDROCHLORIDE 75 mg/1 360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)
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)
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)
68071-2577-3 68071-2577 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20211117 N/A ANDA ANDA076143 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)
68071-2577-9 68071-2577 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20250123 N/A ANDA ANDA076143 NuCare Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)
60687-340-01 60687-340 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20180201 N/A ANDA ANDA076143 American Health Packaging BUPROPION HYDROCHLORIDE 75 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-340-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-340-11)
0904-6635-61 0904-6635 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20060117 N/A ANDA ANDA076143 Major Pharmaceuticals BUPROPION HYDROCHLORIDE 75 mg/1 100 BLISTER PACK in 1 CARTON (0904-6635-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60429-746-01 60429-746 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA076143 Golden State Medical Supply, Inc. BUPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60429-746-01)
60429-747-01 60429-747 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion Hydrochloride TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA076143 Golden State Medical Supply, Inc. BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60429-747-01)
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)
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