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
70771-1774-6	70771-1774	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline	TABLET, FILM COATED	ORAL	20230613	N/A	ANDA	ANDA216723	Zydus Lifesciences Limited	VARENICLINE TARTRATE	1 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (70771-1774-6)
70771-1773-6	70771-1773	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline	TABLET, FILM COATED	ORAL	20230613	N/A	ANDA	ANDA216723	Zydus Lifesciences Limited	VARENICLINE TARTRATE	.5 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (70771-1773-6)
70710-1614-6	70710-1614	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline	TABLET, FILM COATED	ORAL	20230613	N/A	ANDA	ANDA216723	Zydus Pharmaceuticals USA Inc.	VARENICLINE TARTRATE	1 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (70710-1614-6)
70710-1613-6	70710-1613	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline	TABLET, FILM COATED	ORAL	20230613	N/A	ANDA	ANDA216723	Zydus Pharmaceuticals USA Inc.	VARENICLINE TARTRATE	.5 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (70710-1613-6)