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
63548-0739-3	63548-0739	HUMAN OTC DRUG	Indoor outdoor allergies	Cetirizine HCl	TABLET	ORAL	20190701	N/A	ANDA	ANDA077946	PLD Acquisitions LLC DBA Avéma Pharma Solutions	CETIRIZINE HYDROCHLORIDE	10 mg/1	1 BOTTLE, PLASTIC in 1 BOX (63548-0739-3) / 300 TABLET in 1 BOTTLE, PLASTIC
55910-039-45	55910-039	HUMAN OTC DRUG	All Day Allergy Relief	Cetirizine HCL	TABLET	ORAL	20190701	N/A	ANDA	ANDA077946	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	CETIRIZINE HYDROCHLORIDE	10 mg/1	1 BOTTLE, PLASTIC in 1 BOX (55910-039-45) / 45 TABLET in 1 BOTTLE, PLASTIC
59726-739-05	59726-739	HUMAN OTC DRUG	All Day Allergy	Cetirizine HCL	TABLET	ORAL	20190701	20241227	ANDA	ANDA077946	P & L Development, LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	5 BLISTER PACK in 1 CARTON (59726-739-05) / 1 TABLET in 1 BLISTER PACK
59726-739-14	59726-739	HUMAN OTC DRUG	All Day Allergy	Cetirizine HCL	TABLET	ORAL	20190701	20241227	ANDA	ANDA077946	P & L Development, LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	14 BLISTER PACK in 1 CARTON (59726-739-14) / 1 TABLET in 1 BLISTER PACK
0781-1683-01	0781-1683	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20071227	N/A	ANDA	ANDA077946	Sandoz Inc	CETIRIZINE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (0781-1683-01)
0781-1683-64	0781-1683	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20071227	N/A	ANDA	ANDA077946	Sandoz Inc	CETIRIZINE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOX, UNIT-DOSE (0781-1683-64)
0781-1684-01	0781-1684	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20071227	N/A	ANDA	ANDA077946	Sandoz Inc	CETIRIZINE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (0781-1684-01)
0781-1684-64	0781-1684	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride	TABLET	ORAL	20071227	N/A	ANDA	ANDA077946	Sandoz Inc	CETIRIZINE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOX, UNIT-DOSE (0781-1684-64)