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
51407-615-05	51407-615	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20211203	N/A	ANDA	ANDA209603	Golden State Medical Supply, Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51407-615-05)
51407-616-01	51407-616	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20211203	N/A	ANDA	ANDA209603	Golden State Medical Supply, Inc.	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51407-616-01)
55154-0181-0	55154-0181	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250506	N/A	ANDA	ANDA209603	Cardinal Health 107, LLC	LABETALOL HYDROCHLORIDE	100 mg/1	10 BLISTER PACK in 1 BAG (55154-0181-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-0182-0	55154-0182	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250506	N/A	ANDA	ANDA209603	Cardinal Health 107, LLC	LABETALOL HYDROCHLORIDE	200 mg/1	10 BLISTER PACK in 1 BAG (55154-0182-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-0184-0	55154-0184	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250506	N/A	ANDA	ANDA209603	Cardinal Health 107, LLC	LABETALOL HYDROCHLORIDE	300 mg/1	10 BLISTER PACK in 1 BAG (55154-0184-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
51407-615-01	51407-615	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20211203	N/A	ANDA	ANDA209603	Golden State Medical Supply, Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51407-615-01)
51407-614-05	51407-614	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20211203	N/A	ANDA	ANDA209603	Golden State Medical Supply, Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51407-614-05)
51407-614-01	51407-614	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20211203	N/A	ANDA	ANDA209603	Golden State Medical Supply, Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51407-614-01)
0615-8512-39	0615-8512	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240614	N/A	ANDA	ANDA209603	NCS HealthCare of KY, LLC dba Vangard Labs	LABETALOL HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8512-39)
0615-8513-39	0615-8513	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240618	N/A	ANDA	ANDA209603	NCS HealthCare of KY, LLC dba Vangard Labs	LABETALOL HYDROCHLORIDE	200 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8513-39)
51655-322-25	51655-322	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20230425	N/A	ANDA	ANDA209603	Northwind Health Company, LLC	LABETALOL HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-322-25)
70518-3993-1	70518-3993	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240124	N/A	ANDA	ANDA209603	REMEDYREPACK INC.	LABETALOL HYDROCHLORIDE	200 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-1)
70518-3993-2	70518-3993	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20250120	N/A	ANDA	ANDA209603	REMEDYREPACK INC.	LABETALOL HYDROCHLORIDE	200 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-2)
70518-3993-0	70518-3993	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240124	N/A	ANDA	ANDA209603	REMEDYREPACK INC.	LABETALOL HYDROCHLORIDE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-0)
71335-2434-2	71335-2434	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240715	N/A	ANDA	ANDA209603	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2434-2)
71335-2434-5	71335-2434	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240715	N/A	ANDA	ANDA209603	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-2434-5)
71335-2434-3	71335-2434	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240715	N/A	ANDA	ANDA209603	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	58 TABLET, FILM COATED in 1 BOTTLE (71335-2434-3)
67296-2114-6	67296-2114	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20210527	N/A	ANDA	ANDA209603	RedPharm Drug	LABETALOL HYDROCHLORIDE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)
71335-2434-1	71335-2434	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240715	N/A	ANDA	ANDA209603	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2434-1)
71335-2434-4	71335-2434	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20240715	N/A	ANDA	ANDA209603	Bryant Ranch Prepack	LABETALOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2434-4)