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=ANDA210497"
符合检索条件的记录共 59 条，共 3 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
71335-1044-1 71335-1044 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20190103 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-1)
71335-1044-2 71335-1044 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200610 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-2)
71335-1044-3 71335-1044 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20190228 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-3)
72189-124-30 72189-124 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200814 N/A ANDA ANDA210497 DIRECT RX BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-124-30)
72189-134-72 72189-134 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201015 N/A ANDA ANDA210497 DIRECT RX BUPROPION HYDROCHLORIDE 150 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-72)
72189-134-90 72189-134 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201015 N/A ANDA ANDA210497 DIRECT RX BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-90)
72189-124-72 72189-124 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200814 N/A ANDA ANDA210497 DIRECT RX BUPROPION HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-124-72)
72189-134-30 72189-134 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201015 N/A ANDA ANDA210497 DIRECT RX BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-30)
72189-134-60 72189-134 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201015 N/A ANDA ANDA210497 DIRECT RX BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60)
71335-1214-1 71335-1214 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20190503 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1)
71335-1214-5 71335-1214 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240809 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5)
71335-1214-6 71335-1214 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240809 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)
71335-1214-2 71335-1214 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210422 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2)
71335-1214-3 71335-1214 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20190610 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3)
71335-1214-4 71335-1214 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20190529 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4)
70518-2458-0 70518-2458 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20191129 N/A ANDA ANDA210497 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-0)
70518-2458-2 70518-2458 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200706 N/A ANDA ANDA210497 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-2)
80425-0300-3 80425-0300 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230406 N/A ANDA ANDA210497 Advanced Rx Pharmacy of Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-3)
80425-0300-1 80425-0300 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230406 N/A ANDA ANDA210497 Advanced Rx Pharmacy of Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-1)
80425-0300-2 80425-0300 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230406 N/A ANDA ANDA210497 Advanced Rx Pharmacy of Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-2)
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