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
82804-204-30	82804-204	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	levocetirizine dihydrochloride	TABLET	ORAL	20250307	N/A	ANDA	ANDA090385	Proficient Rx LP	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (82804-204-30)
68071-3841-9	68071-3841	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	levocetirizine dihydrochloride	TABLET	ORAL	20250507	N/A	ANDA	ANDA090385	NuCare Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET in 1 BOTTLE (68071-3841-9)
68462-346-90	68462-346	HUMAN PRESCRIPTION DRUG	LEVOCETIRIZINE DIHYDROCHLORIDE	levocetirizine dihydrochloride	TABLET	ORAL	20110225	N/A	ANDA	ANDA090385	Glenmark Pharmaceuticals Inc., USA	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET in 1 BOTTLE (68462-346-90)