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
72162-2019-1	72162-2019	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20240403	N/A	ANDA	ANDA091159	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (72162-2019-1)
72162-2019-6	72162-2019	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20240403	N/A	ANDA	ANDA091159	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (72162-2019-6)
72162-2086-1	72162-2086	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20240403	N/A	ANDA	ANDA091159	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (72162-2086-1)
72162-2087-1	72162-2087	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20240403	N/A	ANDA	ANDA091159	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (72162-2087-1)
0115-1800-01	0115-1800	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20140407	N/A	ANDA	ANDA091159	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0115-1800-01)
0115-1801-01	0115-1801	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20140407	N/A	ANDA	ANDA091159	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0115-1801-01)
0115-1802-01	0115-1802	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET	ORAL	20140407	N/A	ANDA	ANDA091159	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0115-1802-01)