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
62135-603-60	62135-603	HUMAN PRESCRIPTION DRUG	Risperidone	Risperidone	TABLET, FILM COATED	ORAL	20231229	N/A	ANDA	ANDA077543	Chartwell RX, LLC	RISPERIDONE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-603-60)
62135-600-60	62135-600	HUMAN PRESCRIPTION DRUG	Risperidone	Risperidone	TABLET, FILM COATED	ORAL	20231229	N/A	ANDA	ANDA077543	Chartwell RX, LLC	RISPERIDONE	.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-600-60)
62135-604-60	62135-604	HUMAN PRESCRIPTION DRUG	Risperidone	Risperidone	TABLET, FILM COATED	ORAL	20231229	N/A	ANDA	ANDA077543	Chartwell RX, LLC	RISPERIDONE	3 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-604-60)
62135-601-60	62135-601	HUMAN PRESCRIPTION DRUG	Risperidone	Risperidone	TABLET, FILM COATED	ORAL	20231229	N/A	ANDA	ANDA077543	Chartwell RX, LLC	RISPERIDONE	.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-601-60)
62135-605-60	62135-605	HUMAN PRESCRIPTION DRUG	Risperidone	Risperidone	TABLET, FILM COATED	ORAL	20231229	N/A	ANDA	ANDA077543	Chartwell RX, LLC	RISPERIDONE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-605-60)
62135-602-60	62135-602	HUMAN PRESCRIPTION DRUG	Risperidone	Risperidone	TABLET, FILM COATED	ORAL	20231229	N/A	ANDA	ANDA077543	Chartwell RX, LLC	RISPERIDONE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-602-60)