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
0363-1847-95	0363-1847	HUMAN OTC DRUG	Allergy Relief	fexofenadine hydrochloride	TABLET, FILM COATED	ORAL	20240201	N/A	ANDA	ANDA212971	Walgreen Company	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (0363-1847-95) / 45 TABLET, FILM COATED in 1 BOTTLE
72288-847-39	72288-847	HUMAN OTC DRUG	basic care allergy	fexofenadine hydrochloride	TABLET, FILM COATED	ORAL	20210816	N/A	ANDA	ANDA212971	Amazon.com Services LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (72288-847-39) / 30 TABLET, FILM COATED in 1 BOTTLE
72288-847-47	72288-847	HUMAN OTC DRUG	basic care allergy	fexofenadine hydrochloride	TABLET, FILM COATED	ORAL	20210816	N/A	ANDA	ANDA212971	Amazon.com Services LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	150 TABLET, FILM COATED in 1 BOTTLE (72288-847-47)
71205-739-30	71205-739	HUMAN OTC DRUG	Fexofenadine Hydrochloride	fexofenadine hydrochloride	TABLET, FILM COATED	ORAL	20221228	N/A	ANDA	ANDA212971	Proficient Rx LP	FEXOFENADINE HYDROCHLORIDE	180 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-739-30)
71205-739-60	71205-739	HUMAN OTC DRUG	Fexofenadine Hydrochloride	fexofenadine hydrochloride	TABLET, FILM COATED	ORAL	20221228	N/A	ANDA	ANDA212971	Proficient Rx LP	FEXOFENADINE HYDROCHLORIDE	180 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-739-60)
71205-739-90	71205-739	HUMAN OTC DRUG	Fexofenadine Hydrochloride	fexofenadine hydrochloride	TABLET, FILM COATED	ORAL	20221228	N/A	ANDA	ANDA212971	Proficient Rx LP	FEXOFENADINE HYDROCHLORIDE	180 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-739-90)
82442-300-72	82442-300	HUMAN OTC DRUG	up and up non drowsy allergy relief	fexofenadine hydrochloride	TABLET, COATED	ORAL	20240304	N/A	ANDA	ANDA212971	Target Corporation	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (82442-300-72) / 60 TABLET, COATED in 1 BOTTLE