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
59762-0057-1	59762-0057	HUMAN PRESCRIPTION DRUG	Alprazolam XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA AUTHORIZED GENERIC	NDA021434	Greenstone LLC	ALPRAZOLAM	.5 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0057-1)
59762-0059-1	59762-0059	HUMAN PRESCRIPTION DRUG	Alprazolam XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA AUTHORIZED GENERIC	NDA021434	Greenstone LLC	ALPRAZOLAM	1 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0059-1)
59762-0066-1	59762-0066	HUMAN PRESCRIPTION DRUG	Alprazolam XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA AUTHORIZED GENERIC	NDA021434	Greenstone LLC	ALPRAZOLAM	2 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0066-1)
59762-0068-1	59762-0068	HUMAN PRESCRIPTION DRUG	Alprazolam XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA AUTHORIZED GENERIC	NDA021434	Greenstone LLC	ALPRAZOLAM	3 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0068-1)
0009-0057-07	0009-0057	HUMAN PRESCRIPTION DRUG	Xanax XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA	NDA021434	PHARMACIA & UPJOHN COMPANY LLC	ALPRAZOLAM	.5 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0057-07)
0009-0059-07	0009-0059	HUMAN PRESCRIPTION DRUG	Xanax XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA	NDA021434	PHARMACIA & UPJOHN COMPANY LLC	ALPRAZOLAM	1 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0059-07)
0009-0066-07	0009-0066	HUMAN PRESCRIPTION DRUG	Xanax XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA	NDA021434	PHARMACIA & UPJOHN COMPANY LLC	ALPRAZOLAM	2 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0066-07)
0009-0068-07	0009-0068	HUMAN PRESCRIPTION DRUG	Xanax XR	alprazolam	TABLET, EXTENDED RELEASE	ORAL	20030117	N/A	NDA	NDA021434	PHARMACIA & UPJOHN COMPANY LLC	ALPRAZOLAM	3 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0068-07)