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=ANDA204452"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
43975-352-03 43975-352 HUMAN PRESCRIPTION DRUG PALIPERIDONE PALIPERIDONE TABLET, EXTENDED RELEASE ORAL 20191127 N/A ANDA ANDA204452 ANI Pharmaceuticals, Inc. PALIPERIDONE 9 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-352-03)
43975-351-03 43975-351 HUMAN PRESCRIPTION DRUG PALIPERIDONE PALIPERIDONE TABLET, EXTENDED RELEASE ORAL 20191127 N/A ANDA ANDA204452 ANI Pharmaceuticals, Inc. PALIPERIDONE 6 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-351-03)
43975-349-03 43975-349 HUMAN PRESCRIPTION DRUG PALIPERIDONE PALIPERIDONE TABLET, EXTENDED RELEASE ORAL 20191127 N/A ANDA ANDA204452 ANI Pharmaceuticals, Inc. PALIPERIDONE 1.5 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-349-03)
43975-350-03 43975-350 HUMAN PRESCRIPTION DRUG PALIPERIDONE PALIPERIDONE TABLET, EXTENDED RELEASE ORAL 20191127 N/A ANDA ANDA204452 ANI Pharmaceuticals, Inc. PALIPERIDONE 3 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43975-350-03)
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