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
60687-112-21	60687-112	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20160203	N/A	ANDA	ANDA078921	American Health Packaging	ANASTROZOLE	1 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-112-21) / 1 TABLET, COATED in 1 BLISTER PACK (60687-112-11)
68001-155-08	68001-155	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20140101	N/A	ANDA	ANDA078921	BluePoint Laboratories	ANASTROZOLE	1 mg/1	1000 TABLET, COATED in 1 BOTTLE (68001-155-08)
68001-155-04	68001-155	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20140101	N/A	ANDA	ANDA078921	BluePoint Laboratories	ANASTROZOLE	1 mg/1	30 TABLET, COATED in 1 BOTTLE (68001-155-04)
65841-743-10	65841-743	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20100627	N/A	ANDA	ANDA078921	Zydus Lifesciences Limited	ANASTROZOLE	1 mg/1	1000 TABLET, COATED in 1 BOTTLE (65841-743-10)
65841-743-06	65841-743	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20100627	N/A	ANDA	ANDA078921	Zydus Lifesciences Limited	ANASTROZOLE	1 mg/1	30 TABLET, COATED in 1 BOTTLE (65841-743-06)
68382-209-10	68382-209	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20100627	N/A	ANDA	ANDA078921	Zydus Pharmaceuticals USA Inc.	ANASTROZOLE	1 mg/1	1000 TABLET, COATED in 1 BOTTLE (68382-209-10)
72789-342-15	72789-342	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20230901	N/A	ANDA	ANDA078921	PD-Rx Pharmaceuticals, Inc.	ANASTROZOLE	1 mg/1	15 TABLET, COATED in 1 BOTTLE, PLASTIC (72789-342-15)
68382-209-06	68382-209	HUMAN PRESCRIPTION DRUG	Anastrozole	Anastrozole	TABLET, COATED	ORAL	20100627	N/A	ANDA	ANDA078921	Zydus Pharmaceuticals USA Inc.	ANASTROZOLE	1 mg/1	30 TABLET, COATED in 1 BOTTLE (68382-209-06)