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
69539-127-30	69539-127	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210413	N/A	ANDA	ANDA213226	MSN LABORATORIES PRIVATE LIMITED	PREGABALIN	82.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69539-127-30)
69539-128-30	69539-128	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210413	N/A	ANDA	ANDA213226	MSN LABORATORIES PRIVATE LIMITED	PREGABALIN	165 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69539-128-30)
69539-129-30	69539-129	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210413	N/A	ANDA	ANDA213226	MSN LABORATORIES PRIVATE LIMITED	PREGABALIN	330 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69539-129-30)
72205-079-30	72205-079	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210413	N/A	ANDA	ANDA213226	Novadoz Pharmaceuticals LLC	PREGABALIN	330 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-079-30)
72205-078-30	72205-078	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210413	N/A	ANDA	ANDA213226	Novadoz Pharmaceuticals LLC	PREGABALIN	165 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-078-30)
72205-077-30	72205-077	HUMAN PRESCRIPTION DRUG	PREGABALIN	PREGABALIN	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210413	N/A	ANDA	ANDA213226	Novadoz Pharmaceuticals LLC	PREGABALIN	82.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-077-30)