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=ANDA204890"
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
68001-538-41 68001-538 HUMAN PRESCRIPTION DRUG Pemetrexed Pemetrexed disodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220624 N/A ANDA ANDA204890 BluePoint Laboratories PEMETREXED DISODIUM HEMIPENTAHYDRATE 100 mg/4mL 1 VIAL in 1 CARTON (68001-538-41) / 4 mL in 1 VIAL
68001-539-41 68001-539 HUMAN PRESCRIPTION DRUG Pemetrexed Pemetrexed disodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220624 N/A ANDA ANDA204890 BluePoint Laboratories PEMETREXED DISODIUM HEMIPENTAHYDRATE 500 mg/20mL 1 VIAL in 1 CARTON (68001-539-41) / 20 mL in 1 VIAL
50742-340-01 50742-340 HUMAN PRESCRIPTION DRUG Pemetrexed Pemetrexed disodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220524 N/A ANDA ANDA204890 Ingenus Pharmaceuticals, LLC PEMETREXED DISODIUM HEMIPENTAHYDRATE 100 mg/4mL 1 VIAL in 1 CARTON (50742-340-01) / 4 mL in 1 VIAL
67184-0504-1 67184-0504 HUMAN PRESCRIPTION DRUG Pemetrexed Pemetrexed disodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA204890 Qilu Pharmaceutical Co., Ltd. PEMETREXED DISODIUM HEMIPENTAHYDRATE 500 mg/20mL 1 VIAL in 1 CARTON (67184-0504-1) / 20 mL in 1 VIAL
67184-0503-1 67184-0503 HUMAN PRESCRIPTION DRUG Pemetrexed Pemetrexed disodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220525 N/A ANDA ANDA204890 Qilu Pharmaceutical Co., Ltd. PEMETREXED DISODIUM HEMIPENTAHYDRATE 100 mg/4mL 1 VIAL in 1 CARTON (67184-0503-1) / 4 mL in 1 VIAL
50742-341-01 50742-341 HUMAN PRESCRIPTION DRUG Pemetrexed Pemetrexed disodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20220524 N/A ANDA ANDA204890 Ingenus Pharmaceuticals, LLC PEMETREXED DISODIUM HEMIPENTAHYDRATE 500 mg/20mL 1 VIAL in 1 CARTON (50742-341-01) / 20 mL in 1 VIAL
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