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
0093-5552-01	0093-5552	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20140521	N/A	ANDA	ANDA078908	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	15 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5552-01)
0093-5553-01	0093-5553	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150622	N/A	ANDA	ANDA078908	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5553-01)
0093-5551-01	0093-5551	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150202	N/A	ANDA	ANDA078908	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5551-01)
0093-5550-01	0093-5550	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20141110	N/A	ANDA	ANDA078908	Teva Pharmaceuticals USA, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5550-01)