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
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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
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)
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)
76420-245-90 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 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-90)
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)
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)
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)
71335-1676-1 71335-1676 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200710 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 200 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-1)
71335-1676-2 71335-1676 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200708 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 200 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2)
71335-1676-3 71335-1676 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200813 N/A ANDA ANDA201384 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 200 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3)
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)
47335-860-88 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 (47335-860-88)
63187-597-30 63187-597 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20181201 N/A ANDA ANDA201384 Proficient Rx LP TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-30)
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