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
62207-327-43	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	100 TABLET in 1 BOTTLE (62207-327-43)
62207-327-41	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	24 TABLET in 1 BOTTLE (62207-327-41)
62207-327-47	62207-327	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20210716	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	500 TABLET in 1 BOTTLE (62207-327-47)
62207-729-49	62207-729	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20180608	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	1000 TABLET in 1 BOTTLE (62207-729-49)
62207-761-49	62207-761	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62207-761-49)
62207-762-42	62207-762	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (62207-762-42)
62207-762-43	62207-762	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62207-762-43)
62207-762-47	62207-762	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62207-762-47)
62207-762-49	62207-762	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62207-762-49)
85786-104-24	85786-104	HUMAN OTC DRUG	Dr Simi All Day Pain Relief	Naproxen sodium	TABLET, FILM COATED	ORAL	20250818	N/A	ANDA	ANDA091353	Farmacias De Similares TX LLC	NAPROXEN SODIUM	220 mg/1	24 TABLET, FILM COATED in 1 BOTTLE (85786-104-24)
62207-761-42	62207-761	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (62207-761-42)
62207-761-43	62207-761	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62207-761-43)
62207-761-47	62207-761	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET, FILM COATED	ORAL	20110930	N/A	ANDA	ANDA091353	Granules India Ltd	NAPROXEN SODIUM	220 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62207-761-47)
11673-764-05	11673-764	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20240301	N/A	ANDA	ANDA091353	TARGET CORPORATION	NAPROXEN SODIUM	220 mg/1	50 TABLET in 1 BOTTLE (11673-764-05)
11673-764-09	11673-764	HUMAN OTC DRUG	Naproxen Sodium	Naproxen Sodium	TABLET	ORAL	20240301	N/A	ANDA	ANDA091353	TARGET CORPORATION	NAPROXEN SODIUM	220 mg/1	90 TABLET in 1 BOTTLE (11673-764-09)