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
51079-597-20	51079-597	HUMAN OTC DRUG	Cetirizine Hydrochloride	cetirizine hydrochloride	TABLET, FILM COATED	ORAL	20120330	N/A	ANDA	ANDA076677	Mylan Institutional Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-597-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-597-01)
0378-3635-01	0378-3635	HUMAN OTC DRUG	Cetirizine Hydrochloride	cetirizine hydrochloride	TABLET, FILM COATED	ORAL	20071227	N/A	ANDA	ANDA076677	Mylan Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3635-01)
55154-5399-0	55154-5399	HUMAN OTC DRUG	Cetirizine Hydrochloride	cetirizine hydrochloride	TABLET, FILM COATED	ORAL	20120330	N/A	ANDA	ANDA076677	Cardinal Health 107, LLC	CETIRIZINE HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 BAG (55154-5399-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0378-3637-01	0378-3637	HUMAN OTC DRUG	Cetirizine Hydrochloride	cetirizine hydrochloride	TABLET, FILM COATED	ORAL	20071227	N/A	ANDA	ANDA076677	Mylan Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3637-01)
0378-3637-05	0378-3637	HUMAN OTC DRUG	Cetirizine Hydrochloride	cetirizine hydrochloride	TABLET, FILM COATED	ORAL	20071227	N/A	ANDA	ANDA076677	Mylan Pharmaceuticals Inc.	CETIRIZINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3637-05)