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
55111-782-78	55111-782	HUMAN OTC DRUG	Fexofenadine hydrochloride	Fexofenadine hydrochloride	TABLET	ORAL	20110103	N/A	ANDA	ANDA076502	Dr. Reddy's Laboratories Limited	FEXOFENADINE HYDROCHLORIDE	30 mg/1	10 BLISTER PACK in 1 CARTON (55111-782-78) / 10 TABLET in 1 BLISTER PACK (55111-782-79)
55111-782-90	55111-782	HUMAN OTC DRUG	Fexofenadine hydrochloride	Fexofenadine hydrochloride	TABLET	ORAL	20110103	N/A	ANDA	ANDA076502	Dr. Reddy's Laboratories Limited	FEXOFENADINE HYDROCHLORIDE	30 mg/1	90 TABLET in 1 BOTTLE (55111-782-90)
63868-819-12	63868-819	HUMAN OTC DRUG	Allergy Relief	Fexofenadine Hydrochloride 60 mg	TABLET	ORAL	20210517	N/A	ANDA	ANDA076502	Chain Drug Marketing Association INC	FEXOFENADINE HYDROCHLORIDE	60 mg/1	2 BLISTER PACK in 1 CARTON (63868-819-12) / 6 TABLET in 1 BLISTER PACK
46122-462-75	46122-462	HUMAN OTC DRUG	Allergy Relief	Fexofenadine hydrochloride	TABLET	ORAL	20180220	20260731	ANDA	ANDA076502	AMERISOURCEBERGEN DRUG CORPORATION	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (46122-462-75) / 90 TABLET in 1 BOTTLE
68016-995-03	68016-995	HUMAN OTC DRUG	Fexofenadine Hydrochloride	Fexofenadine hydrochloride	TABLET	ORAL	20140401	N/A	ANDA	ANDA076502	Chain Drug Consortium, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (68016-995-03) / 30 TABLET in 1 BOTTLE
68016-995-45	68016-995	HUMAN OTC DRUG	Fexofenadine Hydrochloride	Fexofenadine hydrochloride	TABLET	ORAL	20140401	N/A	ANDA	ANDA076502	Chain Drug Consortium, LLC	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (68016-995-45) / 45 TABLET in 1 BOTTLE
55910-111-30	55910-111	HUMAN OTC DRUG	Fexofenadine hydrochloride	Fexofenadine hydrochloride	TABLET	ORAL	20190717	N/A	ANDA	ANDA076502	Dollar General	FEXOFENADINE HYDROCHLORIDE	180 mg/1	1 BOTTLE in 1 CARTON (55910-111-30) / 30 TABLET in 1 BOTTLE