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
68382-722-77	68382-722	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, FILM COATED	ORAL	20161027	N/A	ANDA	ANDA205248	Zydus Pharmaceuticals USA Inc.	NATEGLINIDE	120 mg/1	10 BLISTER PACK in 1 CARTON (68382-722-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1015-3	70771-1015	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, FILM COATED	ORAL	20161027	N/A	ANDA	ANDA205248	Zydus Lifesciences Limited	NATEGLINIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1015-3)
70771-1015-1	70771-1015	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, FILM COATED	ORAL	20161027	N/A	ANDA	ANDA205248	Zydus Lifesciences Limited	NATEGLINIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1015-1)
70771-1015-0	70771-1015	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, FILM COATED	ORAL	20161027	N/A	ANDA	ANDA205248	Zydus Lifesciences Limited	NATEGLINIDE	60 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1015-0)