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
50090-1291-1	50090-1291	HUMAN PRESCRIPTION DRUG	Labetalol HCL	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20150806	N/A	ANDA	ANDA200908	A-S Medication Solutions	LABETALOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-1291-1)
71335-1410-1	71335-1410	HUMAN PRESCRIPTION DRUG	Labetalol HCL	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20241007	N/A	ANDA	ANDA200908	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1410-1)
71335-1410-2	71335-1410	HUMAN PRESCRIPTION DRUG	Labetalol HCL	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191127	N/A	ANDA	ANDA200908	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1410-2)
71335-1410-3	71335-1410	HUMAN PRESCRIPTION DRUG	Labetalol HCL	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20241007	N/A	ANDA	ANDA200908	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	58 TABLET, FILM COATED in 1 BOTTLE (71335-1410-3)
71335-1410-4	71335-1410	HUMAN PRESCRIPTION DRUG	Labetalol HCL	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20241007	N/A	ANDA	ANDA200908	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1410-4)
71335-1410-5	71335-1410	HUMAN PRESCRIPTION DRUG	Labetalol HCL	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20241007	N/A	ANDA	ANDA200908	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1410-5)