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=ANDA213761"
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
70752-136-10 70752-136 HUMAN PRESCRIPTION DRUG OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE SOLUTION ORAL 20210602 N/A ANDA ANDA213761 QUAGEN PHARMACEUTICALS LLC OXYCODONE HYDROCHLORIDE 5 mg/5mL 1 BOTTLE, PLASTIC in 1 CARTON (70752-136-10) / 100 mL in 1 BOTTLE, PLASTIC
70752-136-14 70752-136 HUMAN PRESCRIPTION DRUG OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE SOLUTION ORAL 20210602 N/A ANDA ANDA213761 QUAGEN PHARMACEUTICALS LLC OXYCODONE HYDROCHLORIDE 5 mg/5mL 1 BOTTLE, PLASTIC in 1 CARTON (70752-136-14) / 500 mL in 1 BOTTLE, PLASTIC
70752-137-03 70752-137 HUMAN PRESCRIPTION DRUG OXYCODONE HYDROCHLORIDE OXYCODONE HYDROCHLORIDE SOLUTION ORAL 20210602 N/A ANDA ANDA213761 QUAGEN PHARMACEUTICALS LLC OXYCODONE HYDROCHLORIDE 100 mg/5mL 1 BOTTLE in 1 CARTON (70752-137-03) / 30 mL in 1 BOTTLE
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