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
68025-088-30	68025-088	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220623	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	45 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-088-30)
68025-097-10	68025-097	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231101	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	36 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-097-10)
68025-097-30	68025-097	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240812	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	36 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-097-30)
13811-700-30	13811-700	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220623	N/A	NDA	NDA216117	Trigen Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	63 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-700-30)
68025-095-10	68025-095	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231101	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	18 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-095-10)
68025-095-30	68025-095	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240812	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	18 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-095-30)
13811-711-30	13811-711	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220623	N/A	NDA	NDA216117	Trigen Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	45 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-711-30)
68025-084-30	68025-084	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220623	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	72 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-084-30)
68025-096-10	68025-096	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231101	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	27 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-096-10)
68025-096-30	68025-096	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240812	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	27 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-096-30)
68025-089-30	68025-089	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20220623	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	63 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-089-30)
68025-098-10	68025-098	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20231101	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	54 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-098-10)
68025-098-30	68025-098	HUMAN PRESCRIPTION DRUG	RELEXXII	methylphenidate hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20240812	N/A	NDA	NDA216117	Vertical Pharmaceuticals, LLC	METHYLPHENIDATE HYDROCHLORIDE	54 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-098-30)