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
50090-6778-0	50090-6778	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	20231025	N/A	ANDA	ANDA075133	A-S Medication Solutions	LABETALOL HYDROCHLORIDE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)
50090-7156-0	50090-7156	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	20240430	N/A	ANDA	ANDA075133	A-S Medication Solutions	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-0)
50090-7156-1	50090-7156	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	20240430	N/A	ANDA	ANDA075133	A-S Medication Solutions	LABETALOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-1)
0591-0606-01	0591-0606	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	19980803	20260630	ANDA	ANDA075133	Actavis Pharma, Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0606-01)
0591-0607-01	0591-0607	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	19980803	20260531	ANDA	ANDA075133	Actavis Pharma, Inc.	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0607-01)
71205-095-30	71205-095	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA075133	Proficient Rx LP	LABETALOL HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-30)
71205-095-60	71205-095	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA075133	Proficient Rx LP	LABETALOL HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60)
71205-095-90	71205-095	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA075133	Proficient Rx LP	LABETALOL HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-90)
0591-0605-01	0591-0605	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	19980803	20260930	ANDA	ANDA075133	Actavis Pharma, Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-01)
0591-0605-05	0591-0605	HUMAN PRESCRIPTION DRUG	Labetalol hydrochloride	Labetalol hydrochloride	TABLET, FILM COATED	ORAL	19980803	20260930	ANDA	ANDA075133	Actavis Pharma, Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05)