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=ANDA200503"
符合检索条件的记录共 67 条，共 4 页，当前第 3 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
83008-009-30 83008-009 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20230303 20270131 ANDA ANDA200503 Quality Care Products, LLC TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (83008-009-30)
68788-8367-6 68788-8367 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20230201 N/A ANDA ANDA200503 Preferred Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8367-6)
68788-8367-9 68788-8367 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20230201 N/A ANDA ANDA200503 Preferred Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8367-9)
72189-154-30 72189-154 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201110 N/A ANDA ANDA200503 DIRECT RX TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-154-30)
72189-154-60 72189-154 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20201110 N/A ANDA ANDA200503 DIRECT RX TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-154-60)
68788-7601-2 68788-7601 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200206 N/A ANDA ANDA200503 Preferred Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-2)
70518-0942-0 70518-0942 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20180109 N/A ANDA ANDA200503 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0942-0)
70518-0942-2 70518-0942 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240710 N/A ANDA ANDA200503 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0942-2)
68788-7601-3 68788-7601 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200206 N/A ANDA ANDA200503 Preferred Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-3)
68788-7601-6 68788-7601 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200206 N/A ANDA ANDA200503 Preferred Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-6)
68788-7601-9 68788-7601 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200206 N/A ANDA ANDA200503 Preferred Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7601-9)
71205-468-30 71205-468 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200813 N/A ANDA ANDA200503 Proficient Rx LP TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-468-30)
71205-468-60 71205-468 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200813 N/A ANDA ANDA200503 Proficient Rx LP TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-468-60)
71205-468-90 71205-468 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200813 N/A ANDA ANDA200503 Proficient Rx LP TRAMADOL HYDROCHLORIDE 200 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-468-90)
71335-9670-1 71335-9670 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20230324 N/A ANDA ANDA200503 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-1)
68180-698-06 68180-698 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20140819 N/A ANDA ANDA200503 Lupin Pharmaceuticals, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-698-06)
83008-021-30 83008-021 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20230512 20251231 ANDA ANDA200503 Quality Care Products, LLC TRAMADOL HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (83008-021-30)
71335-9670-2 71335-9670 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240403 N/A ANDA ANDA200503 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-2)
71335-9670-3 71335-9670 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240403 N/A ANDA ANDA200503 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-3)
71335-9670-4 71335-9670 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240403 N/A ANDA ANDA200503 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-4)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase