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
68382-189-01	68382-189	HUMAN PRESCRIPTION DRUG	Dipyridamole	Dipyridamole	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA040874	Zydus Pharmaceuticals USA Inc.	DIPYRIDAMOLE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-189-01)
68382-189-05	68382-189	HUMAN PRESCRIPTION DRUG	Dipyridamole	Dipyridamole	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA040874	Zydus Pharmaceuticals USA Inc.	DIPYRIDAMOLE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-189-05)
68382-189-10	68382-189	HUMAN PRESCRIPTION DRUG	Dipyridamole	Dipyridamole	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA040874	Zydus Pharmaceuticals USA Inc.	DIPYRIDAMOLE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-189-10)
68382-189-77	68382-189	HUMAN PRESCRIPTION DRUG	Dipyridamole	Dipyridamole	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA040874	Zydus Pharmaceuticals USA Inc.	DIPYRIDAMOLE	75 mg/1	10 BLISTER PACK in 1 CARTON (68382-189-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK