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"
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
68788-7992-1 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)
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)
71335-1044-1 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)
71335-1044-4 71335-1044 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211228 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-4)
71335-1044-5 71335-1044 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211228 N/A ANDA ANDA210497 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-5)
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)
55700-820-30 55700-820 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20191122 20260831 ANDA ANDA210497 Quality Care Products, LLC BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-30)
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)
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)
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