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
69986-014-01	69986-014	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231130	N/A	ANDA	ANDA214496	Sinotherapeutics Inc.	PREGABALIN	165 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-014-01)
69986-015-01	69986-015	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231130	N/A	ANDA	ANDA214496	Sinotherapeutics Inc.	PREGABALIN	330 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-015-01)
69986-013-01	69986-013	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231130	N/A	ANDA	ANDA214496	Sinotherapeutics Inc.	PREGABALIN	82.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-013-01)