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=ANDA211347"
符合检索条件的记录共 45 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
42806-425-52 42806-425 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230918 N/A ANDA ANDA211347 Epic Pharma, LLC BUPROPION HYDROCHLORIDE 150 mg/1 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-425-52)
42806-425-60 42806-425 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230918 N/A ANDA ANDA211347 Epic Pharma, LLC BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-425-60)
42806-426-01 42806-426 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230918 N/A ANDA ANDA211347 Epic Pharma, LLC BUPROPION HYDROCHLORIDE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-426-01)
42806-426-05 42806-426 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230918 N/A ANDA ANDA211347 Epic Pharma, LLC BUPROPION HYDROCHLORIDE 200 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-426-05)
42806-426-60 42806-426 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230918 N/A ANDA ANDA211347 Epic Pharma, LLC BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-426-60)
71335-1986-1 71335-1986 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20211104 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-1)
71335-1986-2 71335-1986 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-2)
71335-1986-3 71335-1986 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-3)
71335-1986-4 71335-1986 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-4)
71335-1986-5 71335-1986 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-5)
71335-1986-6 71335-1986 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20221229 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 100 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-6)
51655-115-25 51655-115 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20221005 N/A ANDA ANDA211347 Northwind Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-25)
51655-115-26 51655-115 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20221115 N/A ANDA ANDA211347 Northwind Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-26)
51655-115-52 51655-115 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20221130 N/A ANDA ANDA211347 Northwind Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-52)
51655-115-83 51655-115 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230105 N/A ANDA ANDA211347 Northwind Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 150 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-83)
70436-058-02 70436-058 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 100 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-058-02)
70436-058-05 70436-058 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-058-05)
70436-058-01 70436-058 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-058-01)
70436-059-01 70436-059 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 150 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-01)
70436-059-02 70436-059 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02)
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