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
63304-562-01	63304-562	HUMAN PRESCRIPTION DRUG	Acetaminophen and Codeine Phosphate	Acetaminophen and Codeine Phosphate	TABLET	ORAL	19781116	N/A	ANDA	ANDA085868	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; CODEINE PHOSPHATE	300 mg/1; 30 mg/1	100 TABLET in 1 BOTTLE (63304-562-01)
63304-562-05	63304-562	HUMAN PRESCRIPTION DRUG	Acetaminophen and Codeine Phosphate	Acetaminophen and Codeine Phosphate	TABLET	ORAL	19781116	N/A	ANDA	ANDA085868	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; CODEINE PHOSPHATE	300 mg/1; 30 mg/1	500 TABLET in 1 BOTTLE (63304-562-05)
63304-562-10	63304-562	HUMAN PRESCRIPTION DRUG	Acetaminophen and Codeine Phosphate	Acetaminophen and Codeine Phosphate	TABLET	ORAL	19781116	N/A	ANDA	ANDA085868	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; CODEINE PHOSPHATE	300 mg/1; 30 mg/1	1000 TABLET in 1 BOTTLE (63304-562-10)