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=ANDA216550"
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
59651-439-18 59651-439 HUMAN PRESCRIPTION DRUG ESTRADIOL VAGINAL INSERTS Estradiol TABLET, FILM COATED VAGINAL 20240802 N/A ANDA ANDA216550 Aurobindo Pharma Limited ESTRADIOL HEMIHYDRATE 10 ug/1 18 APPLICATOR in 1 CARTON (59651-439-18) / 1 TABLET, FILM COATED in 1 APPLICATOR
59651-439-08 59651-439 HUMAN PRESCRIPTION DRUG ESTRADIOL VAGINAL INSERTS Estradiol TABLET, FILM COATED VAGINAL 20240802 N/A ANDA ANDA216550 Aurobindo Pharma Limited ESTRADIOL HEMIHYDRATE 10 ug/1 8 APPLICATOR in 1 CARTON (59651-439-08) / 1 TABLET, FILM COATED in 1 APPLICATOR
72603-874-18 72603-874 HUMAN PRESCRIPTION DRUG ESTRADIOL VAGINAL INSERTS Estradiol TABLET, FILM COATED VAGINAL 20250901 N/A ANDA ANDA216550 NorthStar Rx LLC ESTRADIOL HEMIHYDRATE 10 ug/1 18 APPLICATOR in 1 CARTON (72603-874-18) / 1 TABLET, FILM COATED in 1 APPLICATOR
72603-874-08 72603-874 HUMAN PRESCRIPTION DRUG ESTRADIOL VAGINAL INSERTS Estradiol TABLET, FILM COATED VAGINAL 20250901 N/A ANDA ANDA216550 NorthStar Rx LLC ESTRADIOL HEMIHYDRATE 10 ug/1 8 APPLICATOR in 1 CARTON (72603-874-08) / 1 TABLET, FILM COATED in 1 APPLICATOR
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