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 56 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
71335-1676-4 71335-1676 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20240404 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 200 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)
68071-2648-3 68071-2648 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220225 N/A ANDA ANDA201384 NuCare Pharmaceuticals,Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2648-3)
35356-790-30 35356-790 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111212 N/A ANDA ANDA201384 Lake Erie Medical DBA Quality Care Products LLC TRAMADOL HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-790-30)
71205-656-30 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 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-30)
71205-656-60 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 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-60)
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)
68071-2732-3 68071-2732 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220525 N/A ANDA ANDA201384 NuCare Pharmaceuticals,Inc. TRAMADOL HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2732-3)
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)
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)
68071-2923-3 68071-2923 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20230126 N/A ANDA ANDA201384 NuCare Pharmaceuticals,Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2923-3)
76420-244-30 76420-244 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220725 N/A ANDA ANDA201384 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-30)
76420-244-60 76420-244 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220725 N/A ANDA ANDA201384 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-60)
76420-244-90 76420-244 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220725 N/A ANDA ANDA201384 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-90)
76420-245-30 76420-245 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220725 N/A ANDA ANDA201384 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-30)
76420-245-60 76420-245 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20220725 N/A ANDA ANDA201384 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-60)
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