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
71247-127-01	71247-127	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210208	N/A	ANDA	ANDA075215	Innogenix, Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71247-127-01)
71247-127-05	71247-127	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210208	N/A	ANDA	ANDA075215	Innogenix, Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71247-127-05)
10135-712-01	10135-712	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA075215	Marlex Pharmaceuticals Inc	LABETALOL	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01)
10135-712-05	10135-712	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA075215	Marlex Pharmaceuticals Inc	LABETALOL	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (10135-712-05)
58657-907-01	58657-907	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	200 mg/1	100 BLISTER PACK in 1 CARTON (58657-907-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (58657-907-10)