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
43602-330-05	43602-330	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Ascent Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	20 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43602-330-05)
43602-330-30	43602-330	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Ascent Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	20 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43602-330-30)
43602-334-05	43602-334	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Ascent Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	40 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43602-334-05)
43602-334-30	43602-334	HUMAN PRESCRIPTION DRUG	DEXMETHYLPHENIDATE HYDROCHLORIDE	dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20211208	N/A	ANDA	ANDA215523	Ascent Pharmaceuticals, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	40 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43602-334-30)