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
42571-122-05	42571-122	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20130930	N/A	ANDA	ANDA202046	Micro Labs Limited	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42571-122-05)
42571-122-30	42571-122	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20130930	N/A	ANDA	ANDA202046	Micro Labs Limited	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42571-122-30)
42571-122-32	42571-122	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20130930	N/A	ANDA	ANDA202046	Micro Labs Limited	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (42571-122-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-122-11)
42571-122-90	42571-122	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20130930	N/A	ANDA	ANDA202046	Micro Labs Limited	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42571-122-90)
10135-639-30	10135-639	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20180901	N/A	ANDA	ANDA202046	Marlex Pharmaceuticals Inc	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (10135-639-30)
10135-639-90	10135-639	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20180901	N/A	ANDA	ANDA202046	Marlex Pharmaceuticals Inc	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (10135-639-90)
68788-7699-1	68788-7699	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA202046	Preferred Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7699-1)
68788-7699-3	68788-7699	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20200402	N/A	ANDA	ANDA202046	Preferred Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7699-3)
68788-7699-6	68788-7699	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA202046	Preferred Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7699-6)
68788-7699-9	68788-7699	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20200401	N/A	ANDA	ANDA202046	Preferred Pharmaceuticals, Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7699-9)
71205-210-30	71205-210	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA202046	Proficient Rx LP	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-210-30)
71205-210-60	71205-210	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA202046	Proficient Rx LP	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-210-60)
71205-210-90	71205-210	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA202046	Proficient Rx LP	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-210-90)
68071-5107-9	68071-5107	HUMAN PRESCRIPTION DRUG	Levocetirizine Dihydrochloride	levocetirizine Dihydrochloride	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA202046	NuCare Pharmaceuticals,Inc.	LEVOCETIRIZINE DIHYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-5107-9)