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
69654-582-30	69654-582	HUMAN PRESCRIPTION DRUG	METADATE CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20240222	N/A	NDA	NDA021259	Aytu BioPharma, Inc.	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69654-582-30)
69654-583-30	69654-583	HUMAN PRESCRIPTION DRUG	METADATE CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20240222	N/A	NDA	NDA021259	Aytu BioPharma, Inc.	METHYLPHENIDATE HYDROCHLORIDE	50 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69654-583-30)
69654-584-30	69654-584	HUMAN PRESCRIPTION DRUG	METADATE CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20240222	N/A	NDA	NDA021259	Aytu BioPharma, Inc.	METHYLPHENIDATE HYDROCHLORIDE	60 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69654-584-30)
69654-581-30	69654-581	HUMAN PRESCRIPTION DRUG	METADATE CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20240222	N/A	NDA	NDA021259	Aytu BioPharma, Inc.	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69654-581-30)
69654-580-30	69654-580	HUMAN PRESCRIPTION DRUG	METADATE CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20240222	N/A	NDA	NDA021259	Aytu BioPharma, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69654-580-30)
69654-579-30	69654-579	HUMAN PRESCRIPTION DRUG	METADATE CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20240222	N/A	NDA	NDA021259	Aytu BioPharma, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69654-579-30)
0527-4579-37	0527-4579	HUMAN PRESCRIPTION DRUG	methylphenidate hydrochloride CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20030812	N/A	NDA AUTHORIZED GENERIC	NDA021259	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4579-37)
0527-4583-37	0527-4583	HUMAN PRESCRIPTION DRUG	methylphenidate hydrochloride CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20060321	N/A	NDA AUTHORIZED GENERIC	NDA021259	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	50 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4583-37)
0527-4584-37	0527-4584	HUMAN PRESCRIPTION DRUG	methylphenidate hydrochloride CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20060321	N/A	NDA AUTHORIZED GENERIC	NDA021259	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	60 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4584-37)
0527-4580-37	0527-4580	HUMAN PRESCRIPTION DRUG	methylphenidate hydrochloride CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20030218	N/A	NDA AUTHORIZED GENERIC	NDA021259	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4580-37)
0527-4581-37	0527-4581	HUMAN PRESCRIPTION DRUG	methylphenidate hydrochloride CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20030722	N/A	NDA AUTHORIZED GENERIC	NDA021259	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4581-37)
0527-4582-37	0527-4582	HUMAN PRESCRIPTION DRUG	methylphenidate hydrochloride CD	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20060321	N/A	NDA AUTHORIZED GENERIC	NDA021259	Lannett Company, Inc.	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4582-37)