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=ANDA215652"
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
62332-681-28 62332-681 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20240911 N/A ANDA ANDA215652 Alembic Pharmaceuticals Inc. ALBENDAZOLE 200 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (62332-681-28)
62332-681-02 62332-681 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20240911 N/A ANDA ANDA215652 Alembic Pharmaceuticals Inc. ALBENDAZOLE 200 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (62332-681-02)
46708-681-28 46708-681 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20240911 N/A ANDA ANDA215652 Alembic Pharmaceuticals Limited ALBENDAZOLE 200 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (46708-681-28)
46708-681-02 46708-681 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20240911 N/A ANDA ANDA215652 Alembic Pharmaceuticals Limited ALBENDAZOLE 200 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (46708-681-02)
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