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
11822-6040-2	11822-6040	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220718	20250103	ANDA	ANDA204872	Rite Aid Corporation	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-5	11822-6040	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220718	N/A	ANDA	ANDA204872	Rite Aid Corporation	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-6	11822-6040	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220718	N/A	ANDA	ANDA204872	Rite Aid Corporation	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-6) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-7	11822-6040	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220718	N/A	ANDA	ANDA204872	Rite Aid Corporation	NAPROXEN SODIUM	220 mg/1	270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-6040-7)
11822-6040-8	11822-6040	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220718	N/A	ANDA	ANDA204872	Rite Aid Corporation	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-9	11822-6040	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20220718	N/A	ANDA	ANDA204872	Rite Aid Corporation	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-9) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
21130-674-52	21130-674	HUMAN OTC DRUG	Naproxen	Naproxen Sodium	TABLET, FILM COATED	ORAL	20231004	N/A	ANDA	ANDA204872	Better Living Brands, LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (21130-674-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
27854-170-01	27854-170	HUMAN OTC DRUG	AnaDent	Naproxen Sodium	TABLET, FILM COATED	ORAL	20170123	N/A	ANDA	ANDA204872	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-20	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)
79903-005-25	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)
79903-005-27	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)
79903-005-30	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-30)
79903-005-75	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (79903-005-75) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-90	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)
79903-005-99	79903-005	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET, FILM COATED	ORAL	20201022	N/A	ANDA	ANDA204872	WALMART INC.	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-99)