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
72162-2113-1	72162-2113	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	19990610	N/A	ANDA	ANDA075191	Bryant Ranch Prepack	PENTOXIFYLLINE	400 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2113-1)
0904-5448-61	0904-5448	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	19990610	N/A	ANDA	ANDA075191	Major Pharmaceuticals	PENTOXIFYLLINE	400 mg/1	100 BLISTER PACK in 1 CARTON (0904-5448-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
60505-0033-6	60505-0033	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	19990610	N/A	ANDA	ANDA075191	Apotex Corp.	PENTOXIFYLLINE	400 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0033-6)
60505-0033-7	60505-0033	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	19990610	N/A	ANDA	ANDA075191	Apotex Corp.	PENTOXIFYLLINE	400 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0033-7)
63629-2910-1	63629-2910	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	20050809	N/A	ANDA	ANDA075191	Bryant Ranch Prepack	PENTOXIFYLLINE	400 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2910-1)
63629-2910-2	63629-2910	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	20241206	N/A	ANDA	ANDA075191	Bryant Ranch Prepack	PENTOXIFYLLINE	400 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2910-2)
63629-2910-3	63629-2910	HUMAN PRESCRIPTION DRUG	PENTOXIFYLLINE	PENTOXIFYLLINE	TABLET, EXTENDED RELEASE	ORAL	20231011	N/A	ANDA	ANDA075191	Bryant Ranch Prepack	PENTOXIFYLLINE	400 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2910-3)