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
63187-443-60	63187-443	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	20140303	N/A	ANDA	ANDA074112	Proficient Rx LP	ALPRAZOLAM	1 mg/1	60 TABLET in 1 BOTTLE (63187-443-60)
63187-443-90	63187-443	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	20140303	N/A	ANDA	ANDA074112	Proficient Rx LP	ALPRAZOLAM	1 mg/1	90 TABLET in 1 BOTTLE (63187-443-90)
80425-0100-1	80425-0100	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	20240711	20270319	ANDA	ANDA074112	Advanced Rx Pharmacy of Tennessee, LLC	ALPRAZOLAM	1 mg/1	30 TABLET in 1 BOTTLE (80425-0100-1)
80425-0100-2	80425-0100	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	19951225	20270319	ANDA	ANDA074112	Advanced Rx Pharmacy of Tennessee, LLC	ALPRAZOLAM	1 mg/1	60 TABLET in 1 BOTTLE (80425-0100-2)
53002-3952-1	53002-3952	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	20210101	N/A	ANDA	ANDA074112	RPK Pharmaceuticals, Inc.	ALPRAZOLAM	.5 mg/1	10 TABLET in 1 BOTTLE (53002-3952-1)
53002-3952-2	53002-3952	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	20210101	N/A	ANDA	ANDA074112	RPK Pharmaceuticals, Inc.	ALPRAZOLAM	.5 mg/1	20 TABLET in 1 BOTTLE (53002-3952-2)
53002-3952-3	53002-3952	HUMAN PRESCRIPTION DRUG	Alprazolam	Alprazolam	TABLET	ORAL	20210101	N/A	ANDA	ANDA074112	RPK Pharmaceuticals, Inc.	ALPRAZOLAM	.5 mg/1	30 TABLET in 1 BOTTLE (53002-3952-3)