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 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
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)
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)
71205-465-30 71205-465 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200729 N/A ANDA ANDA210497 Proficient Rx LP BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-30)
71205-465-60 71205-465 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200729 N/A ANDA ANDA210497 Proficient Rx LP BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-60)
71205-465-90 71205-465 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200729 N/A ANDA ANDA210497 Proficient Rx LP BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-90)
68001-520-03 68001-520 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211213 N/A ANDA ANDA210497 BluePoint Laboratories BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-520-03)
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)
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)
68788-7786-9 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 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-9)
68001-520-04 68001-520 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211213 N/A ANDA ANDA210497 BluePoint Laboratories BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-520-04)
68001-520-05 68001-520 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211213 N/A ANDA ANDA210497 BluePoint Laboratories BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-520-05)
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)
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)
71205-504-30 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 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30)
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