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=ANDA202608"
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
0406-0154-01 0406-0154 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Extended-Release Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20121228 N/A ANDA ANDA202608 SpecGx LLC METHYLPHENIDATE HYDROCHLORIDE 54 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-0154-01)
0406-0127-01 0406-0127 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Extended-Release Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20121228 N/A ANDA ANDA202608 SpecGx LLC METHYLPHENIDATE HYDROCHLORIDE 27 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-0127-01)
0406-0136-01 0406-0136 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Extended-Release Methylphenidate Hydrochloride TABLET, EXTENDED RELEASE ORAL 20121228 N/A ANDA ANDA202608 SpecGx LLC METHYLPHENIDATE HYDROCHLORIDE 36 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-0136-01)
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