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
71335-0418-4	71335-0418	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	LEVOCETIRIZINE DIHYDROCHLORIDE	TABLET, FILM COATED	ORAL	20170830	N/A	ANDA	ANDA205564	Bryant Ranch Prepack	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0418-4)
71335-0418-3	71335-0418	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	LEVOCETIRIZINE DIHYDROCHLORIDE	TABLET, FILM COATED	ORAL	20170830	N/A	ANDA	ANDA205564	Bryant Ranch Prepack	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-0418-3)
71335-0418-2	71335-0418	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	LEVOCETIRIZINE DIHYDROCHLORIDE	TABLET, FILM COATED	ORAL	20170830	N/A	ANDA	ANDA205564	Bryant Ranch Prepack	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0418-2)
71335-0418-1	71335-0418	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	LEVOCETIRIZINE DIHYDROCHLORIDE	TABLET, FILM COATED	ORAL	20170830	N/A	ANDA	ANDA205564	Bryant Ranch Prepack	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0418-1)
33342-200-07	33342-200	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	LEVOCETIRIZINE DIHYDROCHLORIDE	TABLET, FILM COATED	ORAL	20160111	N/A	ANDA	ANDA205564	Macleods Pharmaceuticals Limited	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-200-07)
33342-200-10	33342-200	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	LEVOCETIRIZINE DIHYDROCHLORIDE	TABLET, FILM COATED	ORAL	20160111	N/A	ANDA	ANDA205564	Macleods Pharmaceuticals Limited	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-200-10)