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
0093-7701-98	0093-7701	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	Levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20110906	N/A	ANDA	ANDA090199	Teva Pharmaceuticals USA, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98)
43063-479-30	43063-479	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	Levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20131030	N/A	ANDA	ANDA090199	PD-Rx Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-479-30)
68071-3726-9	68071-3726	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	Levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20241122	N/A	ANDA	ANDA090199	NuCare Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3726-9)