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
75834-335-27	75834-335	HUMAN PRESCRIPTION DRUG	varenicline	varenicline	TABLET, FILM COATED	ORAL	20260302	N/A	ANDA	ANDA217115	Nivagen Pharmaceuticals Inc.	VARENICLINE TARTRATE	1 mg/1	4 BLISTER PACK in 1 CARTON (75834-335-27) / 14 TABLET, FILM COATED in 1 BLISTER PACK
75834-335-28	75834-335	HUMAN PRESCRIPTION DRUG	varenicline	varenicline	TABLET, FILM COATED	ORAL	20260302	N/A	ANDA	ANDA217115	Nivagen Pharmaceuticals Inc.	VARENICLINE TARTRATE	1 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (75834-335-28)
75834-336-24	75834-336	HUMAN PRESCRIPTION DRUG	varenicline	varenicline	KIT		20260302	N/A	ANDA	ANDA217115	Nivagen Pharmaceuticals Inc.			2 BOX in 1 KIT (75834-336-24) / 1 KIT in 1 BOX * 1 BLISTER PACK in 1 BOX (75834-334-25) / 11 TABLET, FILM COATED in 1 BLISTER PACK * 3 BLISTER PACK in 1 BOX (75834-335-26) / 14 TABLET, FILM COATED in 1 BLISTER PACK
75834-334-28	75834-334	HUMAN PRESCRIPTION DRUG	varenicline	varenicline	TABLET, FILM COATED	ORAL	20260302	N/A	ANDA	ANDA217115	Nivagen Pharmaceuticals Inc.	VARENICLINE TARTRATE	.5 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (75834-334-28)