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=NDA210450"
符合检索条件的记录共 4 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
0074-0039-56 0074-0039 HUMAN PRESCRIPTION DRUG Orilissa Elagolix TABLET, FILM COATED ORAL 20180723 N/A NDA NDA210450 AbbVie Inc. ELAGOLIX SODIUM 200 mg/1 4 BLISTER PACK in 1 CARTON (0074-0039-56) / 14 TABLET, FILM COATED in 1 BLISTER PACK
0074-0039-14 0074-0039 HUMAN PRESCRIPTION DRUG Orilissa Elagolix TABLET, FILM COATED ORAL 20180723 N/A NDA NDA210450 AbbVie Inc. ELAGOLIX SODIUM 200 mg/1 1 BLISTER PACK in 1 CARTON (0074-0039-14) / 14 TABLET, FILM COATED in 1 BLISTER PACK
0074-0038-28 0074-0038 HUMAN PRESCRIPTION DRUG Orilissa Elagolix TABLET, FILM COATED ORAL 20180723 N/A NDA NDA210450 AbbVie Inc. ELAGOLIX SODIUM 150 mg/1 4 BLISTER PACK in 1 CARTON (0074-0038-28) / 7 TABLET, FILM COATED in 1 BLISTER PACK
0074-0038-07 0074-0038 HUMAN PRESCRIPTION DRUG Orilissa Elagolix TABLET, FILM COATED ORAL 20180723 N/A NDA NDA210450 AbbVie Inc. ELAGOLIX SODIUM 150 mg/1 1 BLISTER PACK in 1 CARTON (0074-0038-07) / 7 TABLET, FILM COATED in 1 BLISTER PACK
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