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 54 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
70518-3058-0 70518-3058 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20210326 N/A ANDA ANDA211347 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3058-0)
70518-3079-0 70518-3079 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20210426 N/A ANDA ANDA211347 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3079-0)
70518-3079-1 70518-3079 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230214 N/A ANDA ANDA211347 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3079-1)
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)
70436-058-02 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)
70436-059-01 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)
70436-059-05 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 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-05)
70436-059-22 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/1 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-22)
70436-060-01 70436-060 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-01)
70436-060-02 70436-060 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 200 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-02)
70436-060-05 70436-060 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20201102 N/A ANDA ANDA211347 Slate Run Pharmaceuticals, LLC BUPROPION HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-060-05)
70518-3811-0 70518-3811 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230730 N/A ANDA ANDA211347 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3811-0)
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)
71335-1837-1 71335-1837 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20210505 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-1)
71335-1837-2 71335-1837 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride SR bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20220217 N/A ANDA ANDA211347 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase