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）

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
59726-801-03	59726-801	HUMAN OTC DRUG	Allergy Relief	Fexofenadine HCl	TABLET, COATED	ORAL	20210820	20270630	ANDA	ANDA204507	P & L Development, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	3 BLISTER PACK in 1 CARTON (59726-801-03) / 1 TABLET, COATED in 1 BLISTER PACK
59726-801-12	59726-801	HUMAN OTC DRUG	Allergy Relief	Fexofenadine HCl	TABLET, COATED	ORAL	20210820	20270630	ANDA	ANDA204507	P & L Development, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	120 BLISTER PACK in 1 CARTON (59726-801-12) / 1 TABLET, COATED in 1 BLISTER PACK
59726-801-15	59726-801	HUMAN OTC DRUG	Allergy Relief	Fexofenadine HCl	TABLET, COATED	ORAL	20210820	20270630	ANDA	ANDA204507	P & L Development, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	15 BLISTER PACK in 1 CARTON (59726-801-15) / 1 TABLET, COATED in 1 BLISTER PACK
59726-801-30	59726-801	HUMAN OTC DRUG	Allergy Relief	Fexofenadine HCl	TABLET, COATED	ORAL	20210820	20270630	ANDA	ANDA204507	P & L Development, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE, PLASTIC in 1 BOX (59726-801-30) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC
59726-801-70	59726-801	HUMAN OTC DRUG	Allergy Relief	Fexofenadine HCl	TABLET, COATED	ORAL	20210820	20270630	ANDA	ANDA204507	P & L Development, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE, PLASTIC in 1 BOX (59726-801-70) / 70 TABLET, COATED in 1 BOTTLE, PLASTIC
68210-4090-1	68210-4090	HUMAN OTC DRUG	Fexofenadine Hydrochloride	Fexofenadine Hydrochloride	TABLET, FILM COATED	ORAL	20200702	N/A	ANDA	ANDA204507	SPIRIT PHARMACEUTICALS LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	100 TABLET, FILM COATED in 1 PACKAGE (68210-4090-1)