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=ANDA207417"
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
43602-178-05 43602-178 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20210129 N/A ANDA ANDA207417 Ascent Pharmaceuticals, Inc. METHYLPHENIDATE 10 mg/5mL 500 mL in 1 BOTTLE (43602-178-05)
43602-178-25 43602-178 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20210129 N/A ANDA ANDA207417 Ascent Pharmaceuticals, Inc. METHYLPHENIDATE 10 mg/5mL 250 mL in 1 BOTTLE (43602-178-25)
43602-177-05 43602-177 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20210129 N/A ANDA ANDA207417 Ascent Pharmaceuticals, Inc. METHYLPHENIDATE 5 mg/5mL 500 mL in 1 BOTTLE (43602-177-05)
43602-177-25 43602-177 HUMAN PRESCRIPTION DRUG Methylphenidate Hydrochloride Methylphenidate Hydrochloride SOLUTION ORAL 20210129 N/A ANDA ANDA207417 Ascent Pharmaceuticals, Inc. METHYLPHENIDATE 5 mg/5mL 250 mL in 1 BOTTLE (43602-177-25)
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