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=ANDA090460"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
68071-3044-2 68071-3044 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride and Acetaminophen Tramadol Hydrochloride and Acetaminophen TABLET, FILM COATED ORAL 20170310 N/A ANDA ANDA090460 NuCare Pharmaceuticals, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3044-2)
68071-3044-3 68071-3044 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride and Acetaminophen Tramadol Hydrochloride and Acetaminophen TABLET, FILM COATED ORAL 20170310 N/A ANDA ANDA090460 NuCare Pharmaceuticals, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3044-3)
68071-3044-6 68071-3044 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride and Acetaminophen Tramadol Hydrochloride and Acetaminophen TABLET, FILM COATED ORAL 20170310 N/A ANDA ANDA090460 NuCare Pharmaceuticals, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3044-6)
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