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
33342-517-11	33342-517	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA217949	Macleods Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (33342-517-11)
33342-517-15	33342-517	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA217949	Macleods Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (33342-517-15)
33342-515-11	33342-515	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA217949	Macleods Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (33342-515-11)
33342-515-15	33342-515	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA217949	Macleods Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (33342-515-15)
33342-516-11	33342-516	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA217949	Macleods Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (33342-516-11)
33342-516-15	33342-516	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA217949	Macleods Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (33342-516-15)