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
71335-9612-1	71335-9612	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride Tablets	TABLET, FILM COATED	ORAL	20230103	N/A	ANDA	ANDA078343	Bryant Ranch Prepack	CETIRIZINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-9612-1)
68788-8435-3	68788-8435	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride Tablets	TABLET, FILM COATED	ORAL	20230427	N/A	ANDA	ANDA078343	Preferred Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8435-3)
68788-8435-6	68788-8435	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride Tablets	TABLET, FILM COATED	ORAL	20230427	N/A	ANDA	ANDA078343	Preferred Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8435-6)
68788-8435-9	68788-8435	HUMAN OTC DRUG	Cetirizine Hydrochloride	Cetirizine Hydrochloride Tablets	TABLET, FILM COATED	ORAL	20230427	N/A	ANDA	ANDA078343	Preferred Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8435-9)