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 61 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
16729-443-15 16729-443 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20181108 N/A ANDA ANDA210497 Accord Healthcare Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-443-15)
16729-443-16 16729-443 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20181108 N/A ANDA ANDA210497 Accord Healthcare Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-443-16)
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)
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)
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)
71205-504-90 71205-504 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201113 N/A ANDA ANDA210497 Proficient Rx LP BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-90)
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)
70518-2458-6 70518-2458 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240812 N/A ANDA ANDA210497 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-6)
80425-0461-1 80425-0461 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20241218 N/A ANDA ANDA210497 Advanced Rx of Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-1)
80425-0461-2 80425-0461 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20241218 N/A ANDA ANDA210497 Advanced Rx of Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-2)
80425-0461-3 80425-0461 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20241218 N/A ANDA ANDA210497 Advanced Rx of Tennessee, LLC BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-3)
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)
68788-7786-1 68788-7786 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201021 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-1)
68788-7786-3 68788-7786 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201021 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-3)
68788-7786-6 68788-7786 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201021 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-6)
68788-7786-8 68788-7786 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201021 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 150 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-8)
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