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
63629-1162-1	63629-1162	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-1162-1)
63629-1163-1	63629-1163	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-1163-1)
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)
63629-1165-1	63629-1165	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 (63629-1165-1)
63629-1166-1	63629-1166	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 (63629-1166-1)
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)
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)
71335-3065-1	71335-3065	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20260206	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3065-1)
71335-3065-5	71335-3065	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20260206	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-3065-5)
71335-3065-2	71335-3065	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20260206	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-3065-2)
71335-3065-3	71335-3065	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20260206	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-3065-3)
71335-3065-4	71335-3065	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20260206	N/A	ANDA	ANDA075215	Bryant Ranch Prepack	LABETALOL	100 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-3065-4)
58657-602-01	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	100 TABLET, FILM COATED in 1 BOTTLE (58657-602-01)
58657-604-01	58657-604	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (58657-604-01)
58657-604-50	58657-604	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20191122	N/A	ANDA	ANDA075215	Method Pharmaceuticals, LLC	LABETALOL	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (58657-604-50)
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)
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)
50090-6833-1	50090-6833	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20231121	N/A	ANDA	ANDA075215	A-S Medication Solutions	LABETALOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6833-1)