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
70010-042-01	70010-042	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181217	N/A	ANDA	ANDA210992	Granules Pharmaceuticals Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-042-01)
70010-042-03	70010-042	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20221031	N/A	ANDA	ANDA210992	Granules Pharmaceuticals Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-042-03)
51407-528-01	51407-528	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20191114	N/A	ANDA	ANDA210992	Golden State Medical Supply, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-528-01)
51407-527-01	51407-527	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20191114	N/A	ANDA	ANDA210992	Golden State Medical Supply, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-527-01)
70010-043-01	70010-043	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181217	N/A	ANDA	ANDA210992	Granules Pharmaceuticals Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-043-01)
70010-043-03	70010-043	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE	METHYLPHENIDATE HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20221031	N/A	ANDA	ANDA210992	Granules Pharmaceuticals Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-043-03)