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=ANDA205135"
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
57664-606-88 57664-606 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200820 N/A ANDA ANDA205135 Sun Pharmaceutical Industries, Inc. METHYLPHENIDATE HYDROCHLORIDE 18 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-606-88)
57664-609-88 57664-609 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200820 N/A ANDA ANDA205135 Sun Pharmaceutical Industries, Inc. METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-609-88)
57664-608-88 57664-608 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200820 N/A ANDA ANDA205135 Sun Pharmaceutical Industries, Inc. METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-608-88)
57664-607-88 57664-607 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20200820 N/A ANDA ANDA205135 Sun Pharmaceutical Industries, Inc. METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-607-88)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase