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=ANDA208643"
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
68180-524-06 68180-524 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20221019 N/A ANDA ANDA208643 Lupin Pharmaceuticals, Inc. PALIPERIDONE 3 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-524-06)
68180-525-06 68180-525 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20221019 N/A ANDA ANDA208643 Lupin Pharmaceuticals, Inc. PALIPERIDONE 6 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-525-06)
68180-526-06 68180-526 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20221019 N/A ANDA ANDA208643 Lupin Pharmaceuticals, Inc. PALIPERIDONE 9 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-526-06)
68180-523-06 68180-523 HUMAN PRESCRIPTION DRUG Paliperidone Paliperidone TABLET, EXTENDED RELEASE ORAL 20221019 N/A ANDA ANDA208643 Lupin Pharmaceuticals, Inc. PALIPERIDONE 1.5 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-523-06)
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