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
79903-609-20	79903-609	HUMAN OTC DRUG	All Day Back and Muscle Pain Relief	Naproxen sodium	TABLET, COATED	ORAL	20231215	N/A	ANDA	ANDA090545	Walmart Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE
0363-9609-01	0363-9609	HUMAN OTC DRUG	BACK AND MUSCLE PAIN	NAPROXEN	TABLET, COATED	ORAL	20190603	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	100 TABLET, COATED in 1 BOTTLE (0363-9609-01)
0363-9609-09	0363-9609	HUMAN OTC DRUG	BACK AND MUSCLE PAIN	NAPROXEN	TABLET, COATED	ORAL	20210626	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (0363-9609-09) / 90 TABLET, COATED in 1 BOTTLE
0363-9609-20	0363-9609	HUMAN OTC DRUG	BACK AND MUSCLE PAIN	NAPROXEN	TABLET, COATED	ORAL	20260201	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	200 TABLET, COATED in 1 BOTTLE (0363-9609-20)
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)
21130-690-05	21130-690	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20230613	N/A	ANDA	ANDA090545	BETTER LIVING BRANDS LLC.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (21130-690-05) / 50 TABLET in 1 BOTTLE
0363-9608-20	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	200 TABLET, COATED in 1 BOTTLE (0363-9608-20)
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)
41226-609-05	41226-609	HUMAN OTC DRUG	NAPROXEN SODIUM	NAPROXEN SODIUM	TABLET, COATED	ORAL	20210612	N/A	ANDA	ANDA090545	Kroger Company	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (41226-609-05) / 50 TABLET, COATED in 1 BOTTLE
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)
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
0363-9608-61	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	600 TABLET, COATED in 1 BOTTLE (0363-9608-61)
0363-9608-90	0363-9608	HUMAN OTC DRUG	ALL DAY PAIN RELIEF	NAPROXEN SODIUM	TABLET, COATED	ORAL	20220401	N/A	ANDA	ANDA090545	WALGREENS	NAPROXEN SODIUM	220 mg/1	90 TABLET, COATED in 1 BOTTLE (0363-9608-90)
69197-394-24	69197-394	HUMAN OTC DRUG	Naproxen Sodium 220mg	Naproxen Sodium 220mg	TABLET, COATED	ORAL	20141223	N/A	ANDA	ANDA090545	Command Brands, LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (69197-394-24) / 24 TABLET, COATED in 1 BOTTLE
85828-394-92	85828-394	HUMAN OTC DRUG	Naproxen Sodium 220mg	Naproxen Sodium 220mg	TABLET, FILM COATED	ORAL	20260318	N/A	ANDA	ANDA090545	Grocery Outlet	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (85828-394-92) / 90 TABLET, FILM COATED in 1 BOTTLE