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
72162-2426-1	72162-2426	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20241118	N/A	ANDA	ANDA209211	Bryant Ranch Prepack	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (72162-2426-1)
72162-2426-6	72162-2426	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20241118	N/A	ANDA	ANDA209211	Bryant Ranch Prepack	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (72162-2426-6)
75834-328-01	75834-328	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20240503	N/A	ANDA	ANDA209211	Nivagen Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (75834-328-01)
75834-327-01	75834-327	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20240503	N/A	ANDA	ANDA209211	Nivagen Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (75834-327-01)
55466-123-12	55466-123	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20240329	N/A	ANDA	ANDA209211	Neolpharma, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (55466-123-12)
72162-2427-1	72162-2427	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20241118	N/A	ANDA	ANDA209211	Bryant Ranch Prepack	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (72162-2427-1)
55466-122-12	55466-122	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20240329	N/A	ANDA	ANDA209211	Neolpharma, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (55466-122-12)