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
66267-373-20	66267-373	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20171121	N/A	ANDA	ANDA091432	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	20 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-373-20)
66267-373-30	66267-373	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20171121	N/A	ANDA	ANDA091432	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-373-30)
66267-373-60	66267-373	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20171121	N/A	ANDA	ANDA091432	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-373-60)
71205-060-14	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	14 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-14)
71205-060-15	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	15 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-15)
71205-060-20	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	20 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-20)
71205-060-30	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-30)
71205-060-40	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	40 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-40)
71205-060-45	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	45 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-45)
71205-060-60	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-60)
71205-060-90	71205-060	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20180601	N/A	ANDA	ANDA091432	Proficient Rx LP	NAPROXEN	375 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-90)
42494-454-10	42494-454	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20230926	N/A	ANDA	ANDA091432	Cameron Pharmaceuticals	NAPROXEN	500 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (42494-454-10)
72162-2276-1	72162-2276	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20240430	N/A	ANDA	ANDA091432	Bryant Ranch Prepack	NAPROXEN	500 mg/1	100 TABLET in 1 BOTTLE (72162-2276-1)
72789-003-60	72789-003	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20190820	N/A	ANDA	ANDA091432	PD-Rx Pharmaceuticals, Inc.	NAPROXEN	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-003-60)
69097-851-07	69097-851	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20160705	N/A	ANDA	ANDA091432	Cipla USA Inc.	NAPROXEN	375 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-851-07)
42494-453-10	42494-453	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20231006	N/A	ANDA	ANDA091432	Cameron Pharmaceuticals	NAPROXEN	375 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (42494-453-10)
72162-2275-1	72162-2275	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20240430	N/A	ANDA	ANDA091432	Bryant Ranch Prepack	NAPROXEN	375 mg/1	100 TABLET in 1 BOTTLE (72162-2275-1)
69097-852-07	69097-852	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20160705	N/A	ANDA	ANDA091432	Cipla USA Inc.	NAPROXEN	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-07)
69097-852-12	69097-852	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET, DELAYED RELEASE	ORAL	20160705	N/A	ANDA	ANDA091432	Cipla USA Inc.	NAPROXEN	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-12)