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=ANDA201384"
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
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
71205-656-90 71205-656 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220427 N/A ANDA ANDA201384 Proficient Rx LP TRAMADOL HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-90)
71205-708-30 71205-708 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20221031 N/A ANDA ANDA201384 Proficient Rx LP TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30)
71205-708-60 71205-708 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20221031 N/A ANDA ANDA201384 Proficient Rx LP TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60)
71205-708-90 71205-708 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20221031 N/A ANDA ANDA201384 Proficient Rx LP TRAMADOL HYDROCHLORIDE 200 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)
61919-893-30 61919-893 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20150626 N/A ANDA ANDA201384 DIRECT RX TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-30)
61919-893-60 61919-893 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20140101 N/A ANDA ANDA201384 DIRECT RX TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-60)
80425-0141-1 80425-0141 HUMAN PRESCRIPTION DRUG Tramadol HCL ER Tramadol HCL TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0141-1)
80425-0141-2 80425-0141 HUMAN PRESCRIPTION DRUG Tramadol HCL ER Tramadol HCL TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0141-2)
80425-0141-3 80425-0141 HUMAN PRESCRIPTION DRUG Tramadol HCL ER Tramadol HCL TABLET, EXTENDED RELEASE ORAL 20241121 N/A ANDA ANDA201384 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0141-3)
63629-8324-1 63629-8324 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200622 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-1)
63629-8324-2 63629-8324 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20211004 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-2)
63629-8324-3 63629-8324 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240403 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-3)
63629-8324-4 63629-8324 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240403 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-4)
47335-859-08 47335-859 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-08)
47335-859-18 47335-859 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-18)
47335-859-83 47335-859 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-83)
47335-859-88 47335-859 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-88)
47335-860-08 47335-860 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-08)
47335-860-18 47335-860 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-18)
47335-860-83 47335-860 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Sun Pharmaceutical Industries, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-83)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase