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
72603-478-01	72603-478	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	KIT		20240923	N/A	ANDA	ANDA214571	NorthStar RxLLC			1 KIT in 1 CARTON (72603-478-01) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
72603-476-01	72603-476	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	TABLET, FILM COATED	ORAL	20240923	N/A	ANDA	ANDA214571	NorthStar RxLLC	VARENICLINE TARTRATE	.5 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (72603-476-01)
31722-690-31	31722-690	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	KIT		20231023	N/A	ANDA	ANDA214571	Camber Pharmaceuticals, Inc.			1 KIT in 1 CARTON (31722-690-31) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
72603-477-01	72603-477	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	TABLET, FILM COATED	ORAL	20240923	N/A	ANDA	ANDA214571	NorthStar RxLLC	VARENICLINE TARTRATE	1 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (72603-477-01)
31722-678-56	31722-678	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	TABLET, FILM COATED	ORAL	20231023	N/A	ANDA	ANDA214571	Camber Pharmaceuticals, Inc.	VARENICLINE TARTRATE	.5 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)
31722-679-31	31722-679	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	TABLET, FILM COATED	ORAL	20231023	N/A	ANDA	ANDA214571	Camber Pharmaceuticals, Inc.	VARENICLINE TARTRATE	1 mg/1	1 BLISTER PACK in 1 CARTON (31722-679-31) / 56 TABLET, FILM COATED in 1 BLISTER PACK
31722-679-56	31722-679	HUMAN PRESCRIPTION DRUG	Varenicline	Varenicline tartrate	TABLET, FILM COATED	ORAL	20231023	N/A	ANDA	ANDA214571	Camber Pharmaceuticals, Inc.	VARENICLINE TARTRATE	1 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (31722-679-56)