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
46708-805-30	46708-805	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Limited	PALIPERIDONE	6 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-805-30)
62332-804-30	62332-804	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Inc.	PALIPERIDONE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-804-30)
46708-803-30	46708-803	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Limited	PALIPERIDONE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-803-30)
62332-806-30	62332-806	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Inc.	PALIPERIDONE	9 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-806-30)
46708-804-30	46708-804	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Limited	PALIPERIDONE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-804-30)
62332-803-30	62332-803	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Inc.	PALIPERIDONE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-803-30)
46708-806-30	46708-806	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Limited	PALIPERIDONE	9 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-806-30)
62332-805-30	62332-805	HUMAN PRESCRIPTION DRUG	paliperidone	paliperidone	TABLET, EXTENDED RELEASE	ORAL	20240930	N/A	ANDA	ANDA218330	Alembic Pharmaceuticals Inc.	PALIPERIDONE	6 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-805-30)