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
71399-8659-1	71399-8659	HUMAN OTC DRUG	fexofenadine hcl	fexofenadine hcl	TABLET, FILM COATED	ORAL	20211101	N/A	ANDA	ANDA204507	AKRON PHARMA INC	FEXOFENADINE HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71399-8659-1)
71399-8659-5	71399-8659	HUMAN OTC DRUG	fexofenadine hcl	fexofenadine hcl	TABLET, FILM COATED	ORAL	20240202	N/A	ANDA	ANDA204507	AKRON PHARMA INC	FEXOFENADINE HYDROCHLORIDE	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71399-8659-5)
72559-027-22	72559-027	HUMAN OTC DRUG	Curist Allergy Relief	Fexofenadine Hydrochloride 180 mg	TABLET	ORAL	20230330	N/A	ANDA	ANDA204507	Little Pharma, Inc.	FEXOFENADINE HYDROCHLORIDE	180 mg/1	200 TABLET in 1 BOTTLE (72559-027-22)
72559-027-23	72559-027	HUMAN OTC DRUG	Curist Allergy Relief	Fexofenadine Hydrochloride 180 mg	TABLET	ORAL	20240131	N/A	ANDA	ANDA204507	Little Pharma, Inc.	FEXOFENADINE HYDROCHLORIDE	180 mg/1	300 TABLET in 1 BOTTLE (72559-027-23)
72559-027-46	72559-027	HUMAN OTC DRUG	Curist Allergy Relief	Fexofenadine Hydrochloride 180 mg	TABLET	ORAL	20240222	N/A	ANDA	ANDA204507	Little Pharma, Inc.	FEXOFENADINE HYDROCHLORIDE	180 mg/1	30 TABLET in 1 BOTTLE (72559-027-46)
72559-028-40	72559-028	HUMAN OTC DRUG	Curist Hives Relief	Fexofenadine Hydrochloride 180 mg	TABLET	ORAL	20230907	N/A	ANDA	ANDA204507	Little Pharma, Inc.	FEXOFENADINE HYDROCHLORIDE	180 mg/1	60 TABLET in 1 BOTTLE (72559-028-40)