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
50228-464-05	50228-464	HUMAN PRESCRIPTION DRUG	Pregabalin Extended Release	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA215675	ScieGen Pharmaceuticals, INC.	PREGABALIN	330 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-464-05)
50228-464-30	50228-464	HUMAN PRESCRIPTION DRUG	Pregabalin Extended Release	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA215675	ScieGen Pharmaceuticals, INC.	PREGABALIN	330 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-464-30)
50228-462-05	50228-462	HUMAN PRESCRIPTION DRUG	Pregabalin Extended Release	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA215675	ScieGen Pharmaceuticals, INC.	PREGABALIN	82.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-462-05)
50228-462-30	50228-462	HUMAN PRESCRIPTION DRUG	Pregabalin Extended Release	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA215675	ScieGen Pharmaceuticals, INC.	PREGABALIN	82.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-462-30)
50228-463-05	50228-463	HUMAN PRESCRIPTION DRUG	Pregabalin Extended Release	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA215675	ScieGen Pharmaceuticals, INC.	PREGABALIN	165 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-463-05)
50228-463-30	50228-463	HUMAN PRESCRIPTION DRUG	Pregabalin Extended Release	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA215675	ScieGen Pharmaceuticals, INC.	PREGABALIN	165 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-463-30)