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
62175-311-37	62175-311	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20130710	N/A	ANDA	ANDA091695	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	27 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-311-37)
62175-312-37	62175-312	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20130923	N/A	ANDA	ANDA091695	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	36 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-312-37)
62175-310-37	62175-310	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20130710	N/A	ANDA	ANDA091695	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	18 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-310-37)
72162-2395-1	72162-2395	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241104	N/A	ANDA	ANDA091695	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	27 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2395-1)
62175-313-37	62175-313	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20130923	N/A	ANDA	ANDA091695	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	54 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-313-37)
72162-2394-1	72162-2394	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20241104	N/A	ANDA	ANDA091695	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	36 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2394-1)