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)
检索条件:" 注册申请号=ANDA212807"
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
27808-225-01 27808-225 HUMAN PRESCRIPTION DRUG Paliperidone paliperidone TABLET, EXTENDED RELEASE ORAL 20211025 N/A ANDA ANDA212807 Tris Pharma Inc PALIPERIDONE 9 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-225-01)
27808-224-01 27808-224 HUMAN PRESCRIPTION DRUG Paliperidone paliperidone TABLET, EXTENDED RELEASE ORAL 20211025 N/A ANDA ANDA212807 Tris Pharma Inc PALIPERIDONE 6 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-224-01)
27808-223-01 27808-223 HUMAN PRESCRIPTION DRUG Paliperidone paliperidone TABLET, EXTENDED RELEASE ORAL 20211025 N/A ANDA ANDA212807 Tris Pharma Inc PALIPERIDONE 3 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-223-01)
27808-222-01 27808-222 HUMAN PRESCRIPTION DRUG Paliperidone paliperidone TABLET, EXTENDED RELEASE ORAL 20211025 N/A ANDA ANDA212807 Tris Pharma Inc PALIPERIDONE 1.5 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-222-01)
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