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
16714-562-01	16714-562	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-562-01)
16714-566-01	16714-566	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	25 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-566-01)
16714-568-01	16714-568	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	35 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-568-01)
16714-564-01	16714-564	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	15 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-564-01)
16714-563-01	16714-563	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-563-01)
16714-569-01	16714-569	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-569-01)
16714-565-01	16714-565	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-565-01)
16714-567-01	16714-567	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220121	20250731	ANDA	ANDA206734	Northstar Rx LLC	DEXMETHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-567-01)