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=ANDA076772"
符合检索条件的记录共 3 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
62037-726-01 62037-726 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190304 N/A ANDA ANDA076772 Actavis Pharma, Inc. METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-726-01)
62037-725-01 62037-725 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190304 N/A ANDA ANDA076772 Actavis Pharma, Inc. METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-725-01)
62037-734-01 62037-734 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190304 N/A ANDA ANDA076772 Actavis Pharma, Inc. METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-734-01)
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