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
64850-641-12	64850-641	HUMAN PRESCRIPTION DRUG	Acetaminophen and Codeine Phosphate	Acetaminophen and Codeine Phosphate	TABLET	ORAL	20190910	N/A	ANDA	ANDA212418	Elite Laboratories, Inc.	ACETAMINOPHEN; CODEINE PHOSPHATE	300 mg/1; 15 mg/1	120 TABLET in 1 BOTTLE (64850-641-12)
64850-642-12	64850-642	HUMAN PRESCRIPTION DRUG	Acetaminophen and Codeine Phosphate	Acetaminophen and Codeine Phosphate	TABLET	ORAL	20190910	N/A	ANDA	ANDA212418	Elite Laboratories, Inc.	ACETAMINOPHEN; CODEINE PHOSPHATE	300 mg/1; 30 mg/1	120 TABLET in 1 BOTTLE (64850-642-12)
64850-643-12	64850-643	HUMAN PRESCRIPTION DRUG	Acetaminophen and Codeine Phosphate	Acetaminophen and Codeine Phosphate	TABLET	ORAL	20190910	N/A	ANDA	ANDA212418	Elite Laboratories, Inc.	ACETAMINOPHEN; CODEINE PHOSPHATE	300 mg/1; 60 mg/1	120 TABLET in 1 BOTTLE (64850-643-12)