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
31722-230-01	31722-230	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Camber Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-230-01)
31722-236-01	31722-236	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Camber Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-236-01)
31722-234-01	31722-234	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Camber Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-234-01)
31722-235-01	31722-235	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Camber Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	35 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-235-01)