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
16571-803-16	16571-803	HUMAN PRESCRIPTION DRUG	Zolmitriptan	Zolmitriptan	TABLET, FILM COATED	ORAL	20160511	N/A	ANDA	ANDA207021	Rising Pharma Holdings, Inc.	ZOLMITRIPTAN	2.5 mg/1	1 BLISTER PACK in 1 CARTON (16571-803-16) / 6 TABLET, FILM COATED in 1 BLISTER PACK
16571-804-13	16571-804	HUMAN PRESCRIPTION DRUG	Zolmitriptan	Zolmitriptan	TABLET, FILM COATED	ORAL	20160511	N/A	ANDA	ANDA207021	Rising Pharma Holdings, Inc.	ZOLMITRIPTAN	5 mg/1	1 BLISTER PACK in 1 CARTON (16571-804-13) / 3 TABLET, FILM COATED in 1 BLISTER PACK
65862-914-69	65862-914	HUMAN PRESCRIPTION DRUG	Zolmitriptan	Zolmitriptan	TABLET, FILM COATED	ORAL	20160511	N/A	ANDA	ANDA207021	Aurobindo Pharma Limited	ZOLMITRIPTAN	2.5 mg/1	1 BLISTER PACK in 1 CARTON (65862-914-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (65862-914-06)
65862-915-64	65862-915	HUMAN PRESCRIPTION DRUG	Zolmitriptan	Zolmitriptan	TABLET, FILM COATED	ORAL	20160511	N/A	ANDA	ANDA207021	Aurobindo Pharma Limited	ZOLMITRIPTAN	5 mg/1	1 BLISTER PACK in 1 CARTON (65862-915-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (65862-915-03)