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
72819-157-03	72819-157	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220531	N/A	ANDA	ANDA203802	Archis Pharma LLC	PALIPERIDONE	1.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72819-157-03)
72819-158-03	72819-158	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220531	N/A	ANDA	ANDA203802	Archis Pharma LLC	PALIPERIDONE	3 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72819-158-03)
72819-159-03	72819-159	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220531	N/A	ANDA	ANDA203802	Archis Pharma LLC	PALIPERIDONE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72819-159-03)
72819-160-03	72819-160	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220531	N/A	ANDA	ANDA203802	Archis Pharma LLC	PALIPERIDONE	9 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72819-160-03)
0378-3980-93	0378-3980	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150924	20240430	ANDA	ANDA203802	Mylan Pharmaceuticals Inc.	PALIPERIDONE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-3980-93)
70518-3873-0	70518-3873	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230926	N/A	ANDA	ANDA203802	REMEDYREPACK INC.	PALIPERIDONE	3 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3873-0)
70518-3876-0	70518-3876	HUMAN PRESCRIPTION DRUG	Paliperidone	paliperidone	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230926	N/A	ANDA	ANDA203802	REMEDYREPACK INC.	PALIPERIDONE	6 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3876-0)