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
65841-677-01	65841-677	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	375 mg/1	100 TABLET in 1 BOTTLE (65841-677-01)
65841-677-05	65841-677	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	375 mg/1	500 TABLET in 1 BOTTLE (65841-677-05)
65841-677-10	65841-677	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	375 mg/1	1000 TABLET in 1 BOTTLE (65841-677-10)
65841-678-01	65841-678	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	500 mg/1	100 TABLET in 1 BOTTLE (65841-678-01)
65841-678-05	65841-678	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	500 mg/1	500 TABLET in 1 BOTTLE (65841-678-05)
65841-678-10	65841-678	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	500 mg/1	1000 TABLET in 1 BOTTLE (65841-678-10)
68382-012-01	68382-012	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	250 mg/1	100 TABLET in 1 BOTTLE (68382-012-01)
68382-012-10	68382-012	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	250 mg/1	1000 TABLET in 1 BOTTLE (68382-012-10)
68382-013-01	68382-013	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	375 mg/1	100 TABLET in 1 BOTTLE (68382-013-01)
68382-013-05	68382-013	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	375 mg/1	500 TABLET in 1 BOTTLE (68382-013-05)
68382-013-10	68382-013	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	375 mg/1	1000 TABLET in 1 BOTTLE (68382-013-10)
65841-676-01	65841-676	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	250 mg/1	100 TABLET in 1 BOTTLE (65841-676-01)
65841-676-10	65841-676	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20171109	N/A	ANDA	ANDA078620	Zydus Lifesciences Limited	NAPROXEN	250 mg/1	1000 TABLET in 1 BOTTLE (65841-676-10)
68382-014-01	68382-014	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	500 mg/1	100 TABLET in 1 BOTTLE (68382-014-01)
68382-014-05	68382-014	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	500 mg/1	500 TABLET in 1 BOTTLE (68382-014-05)
68382-014-10	68382-014	HUMAN PRESCRIPTION DRUG	Naproxen	Naproxen	TABLET	ORAL	20080919	N/A	ANDA	ANDA078620	Zydus Pharmaceuticals USA Inc.	NAPROXEN	500 mg/1	1000 TABLET in 1 BOTTLE (68382-014-10)