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
0591-3694-19	0591-3694	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	6 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3694-19)
0591-3694-30	0591-3694	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3694-30)
0591-3695-19	0591-3695	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	9 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3695-19)
0591-3695-30	0591-3695	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	9 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3695-30)
0591-3693-30	0591-3693	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	3 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3693-30)
0591-3693-19	0591-3693	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	3 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3693-19)
0591-3692-30	0591-3692	HUMAN PRESCRIPTION DRUG	Paliperidone	Paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	N/A	ANDA	ANDA202645	Actavis Pharma, Inc.	PALIPERIDONE	1.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3692-30)