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）

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
50742-341-01	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
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