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
31722-320-30	31722-320	HUMAN PRESCRIPTION DRUG	PALIPERIDONE	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20230823	N/A	ANDA	ANDA216174	Camber Pharmaceuticals, Inc	PALIPERIDONE	9 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-320-30)
31722-317-30	31722-317	HUMAN PRESCRIPTION DRUG	PALIPERIDONE	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20230823	N/A	ANDA	ANDA216174	Camber Pharmaceuticals, Inc	PALIPERIDONE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-317-30)
31722-318-30	31722-318	HUMAN PRESCRIPTION DRUG	PALIPERIDONE	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20230823	N/A	ANDA	ANDA216174	Camber Pharmaceuticals, Inc	PALIPERIDONE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-318-30)
31722-319-30	31722-319	HUMAN PRESCRIPTION DRUG	PALIPERIDONE	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20230823	N/A	ANDA	ANDA216174	Camber Pharmaceuticals, Inc	PALIPERIDONE	6 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-319-30)