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
58657-602-50	58657-602	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (58657-602-50)
10135-711-01	10135-711	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA075215	Marlex Pharmaceuticals Inc	LABETALOL	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-711-01)
10135-711-05	10135-711	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA075215	Marlex Pharmaceuticals Inc	LABETALOL	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (10135-711-05)
58657-906-01	58657-906	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	100 mg/1	100 BLISTER PACK in 1 CARTON (58657-906-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-906-10)
63629-1161-1	63629-1161	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-1161-1)
72162-1677-1	72162-1677	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-1677-1)
72162-1677-5	72162-1677	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-1677-5)
63629-1164-1	63629-1164	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20201002	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-1164-1)
58657-603-01	58657-603	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (58657-603-01)
58657-603-50	58657-603	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (58657-603-50)