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=ANDA204507"
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
50594-504-30 50594-504 HUMAN OTC DRUG Allergy Relief Fexofenadine HCl TABLET, COATED ORAL 20210430 20260430 ANDA ANDA204507 Big Lots FEXOFENADINE HYDROCHLORIDE 180 mg/1 1 BOTTLE, PLASTIC in 1 BOX (50594-504-30) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC
73581-103-10 73581-103 HUMAN OTC DRUG ALLERGY RELIEF FEXOFENADINE HYDROCHLORIDE TABLET ORAL 20200630 N/A ANDA ANDA204507 YYBA CORP FEXOFENADINE HYDROCHLORIDE 60 mg/1 1 BOTTLE in 1 BOX (73581-103-10) / 100 TABLET in 1 BOTTLE
73581-103-20 73581-103 HUMAN OTC DRUG ALLERGY RELIEF FEXOFENADINE HYDROCHLORIDE TABLET ORAL 20230606 N/A ANDA ANDA204507 YYBA CORP FEXOFENADINE HYDROCHLORIDE 60 mg/1 200 TABLET in 1 BOTTLE (73581-103-20)
63187-921-20 63187-921 HUMAN OTC DRUG Fexofenadine HCl Fexofenadine HCl TABLET, FILM COATED ORAL 20171002 N/A ANDA ANDA204507 Proficient Rx LP FEXOFENADINE HYDROCHLORIDE 180 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (63187-921-20)
63187-921-30 63187-921 HUMAN OTC DRUG Fexofenadine HCl Fexofenadine HCl TABLET, FILM COATED ORAL 20171002 N/A ANDA ANDA204507 Proficient Rx LP FEXOFENADINE HYDROCHLORIDE 180 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-921-30)
63187-921-60 63187-921 HUMAN OTC DRUG Fexofenadine HCl Fexofenadine HCl TABLET, FILM COATED ORAL 20171002 N/A ANDA ANDA204507 Proficient Rx LP FEXOFENADINE HYDROCHLORIDE 180 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-921-60)
63187-921-90 63187-921 HUMAN OTC DRUG Fexofenadine HCl Fexofenadine HCl TABLET, FILM COATED ORAL 20171002 N/A ANDA ANDA204507 Proficient Rx LP FEXOFENADINE HYDROCHLORIDE 180 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-921-90)
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