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
27854-505-01	27854-505	HUMAN OTC DRUG	Flanax Pain Reliever/Fever reducer	Naproxen Sodium	TABLET, COATED	ORAL	20200515	N/A	ANDA	ANDA090545	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (27854-505-01) / 24 TABLET, COATED in 1 BOTTLE
27854-505-02	27854-505	HUMAN OTC DRUG	Flanax Pain Reliever/Fever reducer	Naproxen Sodium	TABLET, COATED	ORAL	20200515	N/A	ANDA	ANDA090545	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (27854-505-02) / 2 TABLET, COATED in 1 BOTTLE
27854-555-01	27854-555	HUMAN OTC DRUG	Belmora Flanax	Naproxen Sodium	TABLET	ORAL	20200914	N/A	ANDA	ANDA090545	Belmora LLC	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (27854-555-01) / 24 TABLET in 1 BOTTLE
27854-555-02	27854-555	HUMAN OTC DRUG	Belmora Flanax	Naproxen Sodium	TABLET	ORAL	20200720	N/A	ANDA	ANDA090545	Belmora LLC	NAPROXEN SODIUM	220 mg/1	40 PACKET in 1 BOX (27854-555-02) / 1 TABLET in 1 PACKET
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)
79903-389-50	79903-389	HUMAN OTC DRUG	All Day Pain Relief	Naproxen Sodium	TABLET	ORAL	20250510	N/A	ANDA	ANDA090545	Walmart Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE in 1 CARTON (79903-389-50) / 50 TABLET in 1 BOTTLE
79903-609-09	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 (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE
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
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)
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)
49483-608-05	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)
49483-609-00	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)