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=ANDA090384"
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
63323-134-10 63323-134 HUMAN PRESCRIPTION DRUG Pemetrexed PEMETREXED DISODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA090384 Fresenius Kabi USA, LLC PEMETREXED DISODIUM 100 mg/4mL 1 VIAL, SINGLE-USE in 1 CARTON (63323-134-10) / 4 mL in 1 VIAL, SINGLE-USE
63323-622-00 63323-622 HUMAN PRESCRIPTION DRUG Pemetrexed PEMETREXED DISODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA090384 Fresenius Kabi USA, LLC PEMETREXED DISODIUM 1 g/40mL 1 VIAL, SINGLE-USE in 1 CARTON (63323-622-00) / 40 mL in 1 VIAL, SINGLE-USE
63323-621-00 63323-621 HUMAN PRESCRIPTION DRUG Pemetrexed PEMETREXED DISODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA090384 Fresenius Kabi USA, LLC PEMETREXED DISODIUM 750 mg/30mL 1 VIAL, SINGLE-USE in 1 CARTON (63323-621-00) / 30 mL in 1 VIAL, SINGLE-USE
63323-450-50 63323-450 HUMAN PRESCRIPTION DRUG Pemetrexed PEMETREXED DISODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA090384 Fresenius Kabi USA, LLC PEMETREXED DISODIUM 500 mg/20mL 1 VIAL, SINGLE-USE in 1 CARTON (63323-450-50) / 20 mL in 1 VIAL, SINGLE-USE
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