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
70771-1152-0	70771-1152	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Lifesciences Limited	FINASTERIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1152-0)
70771-1152-1	70771-1152	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Lifesciences Limited	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1152-1)
70771-1152-3	70771-1152	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Lifesciences Limited	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1152-3)
70771-1152-4	70771-1152	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Lifesciences Limited	FINASTERIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (70771-1152-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68382-074-01	68382-074	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Pharmaceuticals USA Inc.	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-074-01)
68382-074-06	68382-074	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Pharmaceuticals USA Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-074-06)
68382-074-10	68382-074	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Pharmaceuticals USA Inc.	FINASTERIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-074-10)
68382-074-77	68382-074	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA078900	Zydus Pharmaceuticals USA Inc.	FINASTERIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (68382-074-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK