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
63629-2055-1	63629-2055	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210126	N/A	ANDA	ANDA207863	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-2055-1)
63629-2054-1	63629-2054	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210126	N/A	ANDA	ANDA207863	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-2054-1)
63629-2053-1	63629-2053	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210202	N/A	ANDA	ANDA207863	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-2053-1)
71930-035-12	71930-035	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA207863	Eywa Pharma Inc	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71930-035-12)
71930-037-12	71930-037	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA207863	Eywa Pharma Inc	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71930-037-12)
71930-037-52	71930-037	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA207863	Eywa Pharma Inc	LABETALOL HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71930-037-52)
71930-035-52	71930-035	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA207863	Eywa Pharma Inc	LABETALOL HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71930-035-52)
71930-036-12	71930-036	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA207863	Eywa Pharma Inc	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71930-036-12)
71930-036-52	71930-036	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20190524	N/A	ANDA	ANDA207863	Eywa Pharma Inc	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71930-036-52)