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
0363-9609-42	0363-9609	HUMAN OTC DRUG	BACK AND MUSCLE PAIN	NAPROXEN	TABLET, COATED	ORAL	20190605	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	24 TABLET, COATED in 1 BOTTLE (0363-9609-42)
0363-9608-27	0363-9608	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20190630	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	270 TABLET, COATED in 1 BOTTLE (0363-9608-27)
0363-9608-42	0363-9608	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20190630	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (0363-9608-42) / 24 TABLET, COATED in 1 BOTTLE
0363-9608-09	0363-9608	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20210626	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (0363-9608-09) / 90 TABLET, COATED in 1 BOTTLE
53185-394-50	53185-394	HUMAN OTC DRUG	Naproxen Sodium 220mg	Naproxen Sodium 220mg	TABLET, COATED	ORAL	20141223	N/A	ANDA	ANDA090545	Athlete's Needs, Inc.	NAPROXEN SODIUM	220 mg/1	50 TABLET, COATED in 1 BOTTLE (53185-394-50)
0363-6099-01	0363-6099	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20190708	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	100 TABLET, COATED in 1 BOTTLE (0363-6099-01)
0363-6099-05	0363-6099	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20190708	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	50 TABLET, COATED in 1 BOTTLE (0363-6099-05)
0363-6099-20	0363-6099	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20190708	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	200 TABLET, COATED in 1 BOTTLE (0363-6099-20)
53329-688-30	53329-688	HUMAN OTC DRUG	Naproxen Sodium 220mg	Naproxen Sodium	TABLET	ORAL	20180801	N/A	ANDA	ANDA090545	Medline Industries, LP	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (53329-688-30)
49483-608-01	49483-608	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20160328	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-608-01)
49483-609-00	49483-609	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20160328	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	6500 TABLET, FILM COATED in 1 BAG (49483-609-00)
49483-609-01	49483-609	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20160328	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-609-01)
49483-609-05	49483-609	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20160328	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-609-05)
49483-608-05	49483-608	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20160328	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-608-05)
49483-608-31	49483-608	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20230808	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (49483-608-31)
49483-608-00	49483-608	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20160328	N/A	ANDA	ANDA090545	TIME CAP LABORATORIES, INC	NAPROXEN SODIUM	220 mg/1	6500 TABLET, FILM COATED in 1 BAG (49483-608-00)