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=ANDA202102"
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
46708-261-10 46708-261 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20150521 N/A ANDA ANDA202102 Alembic Pharmaceuticals Limited ARIPIPRAZOLE 15 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (46708-261-10)
62332-103-30 62332-103 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20160707 N/A ANDA ANDA202102 Alembic Pharmaceuticals Inc. ARIPIPRAZOLE 10 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (62332-103-30)
62332-104-30 62332-104 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20160707 N/A ANDA ANDA202102 Alembic Pharmaceuticals Inc. ARIPIPRAZOLE 15 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (62332-104-30)
46708-260-10 46708-260 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20150521 N/A ANDA ANDA202102 Alembic Pharmaceuticals Limited ARIPIPRAZOLE 10 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (46708-260-10)
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