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
0078-0371-05	0078-0371	HUMAN PRESCRIPTION DRUG	Ritalin LA	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20020605	20260930	NDA	NDA021284	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0371-05)
0781-2362-01	0781-2362	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20151124	20261130	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2362-01)
0781-2384-01	0781-2384	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20250220	N/A	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2384-01)
0078-0372-05	0078-0372	HUMAN PRESCRIPTION DRUG	Ritalin LA	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20020605	20261031	NDA	NDA021284	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0372-05)
0781-2363-01	0781-2363	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20151124	20270430	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2363-01)
0781-2385-01	0781-2385	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20250610	N/A	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2385-01)
0781-2361-01	0781-2361	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20180228	20260930	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2361-01)
0078-0370-05	0078-0370	HUMAN PRESCRIPTION DRUG	Ritalin LA	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20020605	20261031	NDA	NDA021284	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0370-05)
0781-2383-01	0781-2383	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20250303	N/A	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2383-01)
0078-0424-05	0078-0424	HUMAN PRESCRIPTION DRUG	Ritalin LA	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20020605	20260930	NDA	NDA021284	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0424-05)
0781-2364-01	0781-2364	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20151124	20261031	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2364-01)
0781-2386-01	0781-2386	HUMAN PRESCRIPTION DRUG	Methylphenidate	methylphenidate	CAPSULE, EXTENDED RELEASE	ORAL	20250303	N/A	NDA AUTHORIZED GENERIC	NDA021284	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2386-01)