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
71335-9690-4	71335-9690	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-9690-4)
71335-9690-5	71335-9690	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	300 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-9690-5)
71247-126-01	71247-126	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210208	N/A	ANDA	ANDA075215	Innogenix, Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71247-126-01)
71335-2923-1	71335-2923	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20251029	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71335-2923-1)
71335-2876-1	71335-2876	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20251029	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2876-1)