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
72888-121-05	72888-121	HUMAN PRESCRIPTION DRUG	LABETALOL HYDROCHLORIDE	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210818	N/A	ANDA	ANDA211953	Advagen Pharma Ltd	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72888-121-05)
60760-784-90	60760-784	HUMAN PRESCRIPTION DRUG	LABETALOL HYDROCHLORIDE	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221025	N/A	ANDA	ANDA211953	ST. MARY'S MEDICAL PARK PHARMACY	LABETALOL HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-784-90)
67296-2156-1	67296-2156	HUMAN PRESCRIPTION DRUG	LABETALOL HYDROCHLORIDE	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210818	N/A	ANDA	ANDA211953	Redpharm Drug	LABETALOL HYDROCHLORIDE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (67296-2156-1)
50090-7666-1	50090-7666	HUMAN PRESCRIPTION DRUG	LABETALOL HYDROCHLORIDE	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20251001	N/A	ANDA	ANDA211953	A-S Medication Solutions	LABETALOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7666-1)