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=ANDA219118"
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
70954-784-10 70954-784 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20250107 N/A ANDA ANDA219118 ANI Pharmaceuticals, Inc. NABUMETONE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70954-784-10)
70954-784-20 70954-784 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20250107 N/A ANDA ANDA219118 ANI Pharmaceuticals, Inc. NABUMETONE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70954-784-20)
70954-785-10 70954-785 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20250107 N/A ANDA ANDA219118 ANI Pharmaceuticals, Inc. NABUMETONE 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70954-785-10)
70954-785-20 70954-785 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20250107 N/A ANDA ANDA219118 ANI Pharmaceuticals, Inc. NABUMETONE 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70954-785-20)
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