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
72989-409-30	72989-409	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	PHENDIMETRAZINE TARTRATE	CAPSULE, EXTENDED RELEASE	ORAL	20221101	N/A	NDA	NDA018074	Acertis Pharmaceuticals, LLC	PHENDIMETRAZINE TARTRATE	105 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72989-409-30)
50090-3988-1	50090-3988	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	PHENDIMETRAZINE TARTRATE	CAPSULE, EXTENDED RELEASE	ORAL	20181218	N/A	NDA	NDA018074	A-S Medication Solutions	PHENDIMETRAZINE TARTRATE	105 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-3988-1)
50090-3988-0	50090-3988	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	PHENDIMETRAZINE TARTRATE	CAPSULE, EXTENDED RELEASE	ORAL	20181218	N/A	NDA	NDA018074	A-S Medication Solutions	PHENDIMETRAZINE TARTRATE	105 mg/1	14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-3988-0)
69543-409-11	69543-409	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	PHENDIMETRAZINE TARTRATE	CAPSULE, EXTENDED RELEASE	ORAL	20181113	N/A	NDA	NDA018074	Virtus Pharmaceuticals, LLC	PHENDIMETRAZINE TARTRATE	105 mg/1	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69543-409-11)