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
43598-022-56	43598-022	HUMAN PRESCRIPTION DRUG	varenicline tartrate	varenicline tartrate	KIT	ORAL	20241213	N/A	ANDA	ANDA215931	Dr. Reddys Laboratories Inc.			1 KIT in 1 CARTON (43598-022-56) * 56 TABLET, FILM COATED in 1 BLISTER PACK
43598-908-56	43598-908	HUMAN PRESCRIPTION DRUG	varenicline tartrate	varenicline tartrate	TABLET, FILM COATED	ORAL	20241213	N/A	ANDA	ANDA215931	Dr. Reddys Laboratories Inc.	VARENICLINE TARTRATE	1 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (43598-908-56)
43598-023-53	43598-023	HUMAN PRESCRIPTION DRUG	varenicline tartrate	varenicline tartrate	KIT	ORAL	20241213	N/A	ANDA	ANDA215931	Dr. Reddys Laboratories Inc.			1 KIT in 1 CARTON (43598-023-53) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
43598-907-56	43598-907	HUMAN PRESCRIPTION DRUG	varenicline tartrate	varenicline tartrate	TABLET, FILM COATED	ORAL	20241213	N/A	ANDA	ANDA215931	Dr. Reddys Laboratories Inc.	VARENICLINE TARTRATE	.5 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (43598-907-56)