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=ANDA214023"
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
50742-391-01 50742-391 HUMAN PRESCRIPTION DRUG estrogens, conjugated estrogens, conjugated TABLET, FILM COATED ORAL 20251016 N/A ANDA ANDA214023 Ingenus Pharmaceuticals, LLC ESTROGENS, CONJUGATED 1.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50742-391-01)
50742-391-10 50742-391 HUMAN PRESCRIPTION DRUG estrogens, conjugated estrogens, conjugated TABLET, FILM COATED ORAL 20251016 N/A ANDA ANDA214023 Ingenus Pharmaceuticals, LLC ESTROGENS, CONJUGATED 1.25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (50742-391-10)
50742-390-10 50742-390 HUMAN PRESCRIPTION DRUG estrogens, conjugated estrogens, conjugated TABLET, FILM COATED ORAL 20251016 N/A ANDA ANDA214023 Ingenus Pharmaceuticals, LLC ESTROGENS, CONJUGATED .9 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (50742-390-10)
50742-390-01 50742-390 HUMAN PRESCRIPTION DRUG estrogens, conjugated estrogens, conjugated TABLET, FILM COATED ORAL 20251016 N/A ANDA ANDA214023 Ingenus Pharmaceuticals, LLC ESTROGENS, CONJUGATED .9 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50742-390-01)
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