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
71205-866-64	71205-866	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium Misoprostol	Diclofenac Sodium and Misoprostol	TABLET, DELAYED RELEASE	ORAL	20220307	N/A	ANDA	ANDA205143	Proficient Rx LP	DICLOFENAC SODIUM; MISOPROSTOL	75 mg/1; 200 ug/1	240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-64)
71205-866-72	71205-866	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium Misoprostol	Diclofenac Sodium and Misoprostol	TABLET, DELAYED RELEASE	ORAL	20220307	N/A	ANDA	ANDA205143	Proficient Rx LP	DICLOFENAC SODIUM; MISOPROSTOL	75 mg/1; 200 ug/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-72)
71205-866-90	71205-866	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium Misoprostol	Diclofenac Sodium and Misoprostol	TABLET, DELAYED RELEASE	ORAL	20220307	N/A	ANDA	ANDA205143	Proficient Rx LP	DICLOFENAC SODIUM; MISOPROSTOL	75 mg/1; 200 ug/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-90)
72162-2518-6	72162-2518	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium Misoprostol	diclofenac sodium and misoprostol	TABLET, DELAYED RELEASE	ORAL	20210715	N/A	ANDA	ANDA205143	Bryant Ranch Prepack	DICLOFENAC SODIUM; MISOPROSTOL	50 mg/1; 200 ug/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2518-6)