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=ANDA218514"
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
27241-277-30 27241-277 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20240626 N/A ANDA ANDA218514 Ajanta Pharma USA Inc. PALIPERIDONE 3 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-277-30)
27241-276-30 27241-276 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20240626 N/A ANDA ANDA218514 Ajanta Pharma USA Inc. PALIPERIDONE 1.5 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-276-30)
27241-279-30 27241-279 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20240626 N/A ANDA ANDA218514 Ajanta Pharma USA Inc. PALIPERIDONE 9 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-279-30)
27241-278-30 27241-278 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20240626 N/A ANDA ANDA218514 Ajanta Pharma USA Inc. PALIPERIDONE 6 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-278-30)
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