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
50090-5837-2	50090-5837	HUMAN PRESCRIPTION DRUG	Benzphetamine Hydrochloride	Benzphetamine Hydrochloride	TABLET, FILM COATED	ORAL	20211102	N/A	ANDA	ANDA090346	A-S Medication Solutions	BENZPHETAMINE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5837-2)
50090-5837-1	50090-5837	HUMAN PRESCRIPTION DRUG	Benzphetamine Hydrochloride	Benzphetamine Hydrochloride	TABLET, FILM COATED	ORAL	20211029	N/A	ANDA	ANDA090346	A-S Medication Solutions	BENZPHETAMINE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-5837-1)
50090-5837-0	50090-5837	HUMAN PRESCRIPTION DRUG	Benzphetamine Hydrochloride	Benzphetamine Hydrochloride	TABLET, FILM COATED	ORAL	20211029	N/A	ANDA	ANDA090346	A-S Medication Solutions	BENZPHETAMINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5837-0)
42806-081-01	42806-081	HUMAN PRESCRIPTION DRUG	Benzphetamine Hydrochloride	Benzphetamine Hydrochloride	TABLET, FILM COATED	ORAL	20151216	N/A	ANDA	ANDA090346	Epic Pharma, LLC	BENZPHETAMINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01)
42806-081-05	42806-081	HUMAN PRESCRIPTION DRUG	Benzphetamine Hydrochloride	Benzphetamine Hydrochloride	TABLET, FILM COATED	ORAL	20151216	N/A	ANDA	ANDA090346	Epic Pharma, LLC	BENZPHETAMINE HYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05)
42806-081-30	42806-081	HUMAN PRESCRIPTION DRUG	Benzphetamine Hydrochloride	Benzphetamine Hydrochloride	TABLET, FILM COATED	ORAL	20151216	N/A	ANDA	ANDA090346	Epic Pharma, LLC	BENZPHETAMINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)