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
0093-5046-01	0093-5046	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170705	N/A	ANDA	ANDA202731	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	35 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5046-01)
0093-5045-01	0093-5045	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170705	N/A	ANDA	ANDA202731	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	25 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5045-01)
0093-5554-01	0093-5554	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20140522	N/A	ANDA	ANDA202731	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5554-01)
0093-5562-01	0093-5562	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20131121	N/A	ANDA	ANDA202731	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5562-01)