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 64 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
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)
72789-301-90 72789-301 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220222 N/A ANDA ANDA210497 PD-Rx Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-301-90)
68788-7992-1 68788-7992 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210806 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 300 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-1)
68788-7992-3 68788-7992 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210806 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-3)
68788-7992-6 68788-7992 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210806 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-6)
68788-7992-8 68788-7992 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210806 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-8)
68788-7992-9 68788-7992 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20210806 N/A ANDA ANDA210497 Preferred Pharmaceuticals Inc. BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7992-9)
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)
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)
50090-5163-0 50090-5163 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200923 N/A ANDA ANDA210497 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-0)
50090-5163-1 50090-5163 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200923 N/A ANDA ANDA210497 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-1)
50090-5163-2 50090-5163 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200923 N/A ANDA ANDA210497 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-2)
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