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=ANDA217229"
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
57664-710-83 57664-710 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20241220 N/A ANDA ANDA217229 Sun Pharmaceutical Industries, Inc. METHYLPHENIDATE HYDROCHLORIDE 72 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-83)
57664-710-88 57664-710 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20241220 N/A ANDA ANDA217229 Sun Pharmaceutical Industries, Inc. METHYLPHENIDATE HYDROCHLORIDE 72 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-88)
72603-399-01 72603-399 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250201 N/A ANDA ANDA217229 Northstar Rx LLC METHYLPHENIDATE HYDROCHLORIDE 72 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72603-399-01)
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