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
68210-0119-3	68210-0119	HUMAN OTC DRUG	CABINET Allergy Relief	Cetirizine Hydrochloride	TABLET, FILM COATED	ORAL	20200310	N/A	ANDA	ANDA209274	Spirit Pharmaceutical LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
70010-163-05	70010-163	HUMAN OTC DRUG	Cetirizine hydrochloride	Cetirizine hydrochloride	TABLET, COATED	ORAL	20220113	N/A	ANDA	ANDA209274	Granules Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	500 TABLET, COATED in 1 BOTTLE (70010-163-05)
70010-163-09	70010-163	HUMAN OTC DRUG	Cetirizine hydrochloride	Cetirizine hydrochloride	TABLET, COATED	ORAL	20220426	N/A	ANDA	ANDA209274	Granules Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE (70010-163-09)
82725-1003-1	82725-1003	HUMAN OTC DRUG	ValuMeds 24-Hour Allergy Relief	CETIRIZINE HYDROCHLORIDE	TABLET	ORAL	20241101	N/A	ANDA	ANDA209274	Cabinet Health P.B.C.	CETIRIZINE HYDROCHLORIDE	10 mg/1	300 TABLET in 1 BOTTLE (82725-1003-1)