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
68071-4006-5	68071-4006	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20170717	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	15 TABLET in 1 BOTTLE (68071-4006-5)
68071-4006-6	68071-4006	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20170717	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	60 TABLET in 1 BOTTLE (68071-4006-6)
68071-4006-7	68071-4006	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20170717	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	14 TABLET in 1 BOTTLE (68071-4006-7)
68071-4006-9	68071-4006	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20170717	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	90 TABLET in 1 BOTTLE (68071-4006-9)
72189-136-14	72189-136	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20201015	N/A	ANDA	ANDA091416	DIRECT RX	NAPROXEN	500 mg/1	14 TABLET in 1 BOTTLE (72189-136-14)
72189-136-20	72189-136	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20201015	N/A	ANDA	ANDA091416	DIRECT RX	NAPROXEN	500 mg/1	20 TABLET in 1 BOTTLE (72189-136-20)
72189-136-30	72189-136	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20201015	N/A	ANDA	ANDA091416	DIRECT RX	NAPROXEN	500 mg/1	30 TABLET in 1 BOTTLE (72189-136-30)
72189-136-60	72189-136	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20201015	N/A	ANDA	ANDA091416	DIRECT RX	NAPROXEN	500 mg/1	60 TABLET in 1 BOTTLE (72189-136-60)
72189-136-71	72189-136	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20201015	N/A	ANDA	ANDA091416	DIRECT RX	NAPROXEN	500 mg/1	100 TABLET in 1 BOTTLE (72189-136-71)
72189-136-90	72189-136	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20201015	N/A	ANDA	ANDA091416	DIRECT RX	NAPROXEN	500 mg/1	90 TABLET in 1 BOTTLE (72189-136-90)
68071-4381-2	68071-4381	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20180406	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	20 TABLET in 1 BOTTLE (68071-4381-2)
68071-4381-4	68071-4381	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20180406	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	4 TABLET in 1 BOTTLE (68071-4381-4)
68071-4381-6	68071-4381	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20180406	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	500 mg/1	6 TABLET in 1 BOTTLE (68071-4381-6)
68071-4510-6	68071-4510	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20180725	N/A	ANDA	ANDA091416	NuCare Pharmaceuticals,Inc.	NAPROXEN	250 mg/1	6 TABLET in 1 BOTTLE (68071-4510-6)
76420-042-01	76420-042	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20200205	N/A	ANDA	ANDA091416	Asclemed USA, Inc.	NAPROXEN	500 mg/1	1 TABLET in 1 BOTTLE, PLASTIC (76420-042-01)
76420-042-02	76420-042	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20200205	N/A	ANDA	ANDA091416	Asclemed USA, Inc.	NAPROXEN	500 mg/1	2 TABLET in 1 BOTTLE, PLASTIC (76420-042-02)
76420-042-10	76420-042	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20200205	N/A	ANDA	ANDA091416	Asclemed USA, Inc.	NAPROXEN	500 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76420-042-10)
76420-042-14	76420-042	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20200205	N/A	ANDA	ANDA091416	Asclemed USA, Inc.	NAPROXEN	500 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (76420-042-14)
76420-042-30	76420-042	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20200205	N/A	ANDA	ANDA091416	Asclemed USA, Inc.	NAPROXEN	500 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (76420-042-30)
76420-042-60	76420-042	HUMAN PRESCRIPTION DRUG	NAPROXEN	NAPROXEN	TABLET	ORAL	20200205	N/A	ANDA	ANDA091416	Asclemed USA, Inc.	NAPROXEN	500 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (76420-042-60)