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
62011-0396-1	62011-0396	HUMAN OTC DRUG	Naproxen Sodium PM	Naproxen Sodium	TABLET	ORAL	20190131	N/A	ANDA	ANDA209726	Strategic Sourcing Services LLC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE, PLASTIC in 1 BOX (62011-0396-1) / 20 TABLET in 1 BOTTLE, PLASTIC
55910-854-20	55910-854	HUMAN OTC DRUG	Naproxen Sodium PM	Naproxen Sodium	TABLET	ORAL	20181231	20250930	ANDA	ANDA209726	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE, PLASTIC in 1 BOX (55910-854-20) / 20 TABLET in 1 BOTTLE, PLASTIC
55910-854-40	55910-854	HUMAN OTC DRUG	Naproxen Sodium PM	Naproxen Sodium	TABLET	ORAL	20181231	20250930	ANDA	ANDA209726	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE, PLASTIC in 1 BOX (55910-854-40) / 40 TABLET in 1 BOTTLE, PLASTIC
70677-0064-1	70677-0064	HUMAN OTC DRUG	Naproxen Sodium PM	Naproxen Sodium	TABLET	ORAL	20181231	N/A	ANDA	ANDA209726	Strategic Sourcing Services LLC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE, PLASTIC in 1 BOX (70677-0064-1) / 20 TABLET in 1 BOTTLE, PLASTIC
69238-1422-2	69238-1422	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine	TABLET, FILM COATED	ORAL	20181023	N/A	ANDA	ANDA209726	Amneal Pharmaceuticals NY LLC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE in 1 CARTON (69238-1422-2) / 20 TABLET, FILM COATED in 1 BOTTLE
69238-1422-4	69238-1422	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine	TABLET, FILM COATED	ORAL	20181023	N/A	ANDA	ANDA209726	Amneal Pharmaceuticals NY LLC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE in 1 CARTON (69238-1422-4) / 40 TABLET, FILM COATED in 1 BOTTLE
69238-1422-6	69238-1422	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine	TABLET, FILM COATED	ORAL	20181023	N/A	ANDA	ANDA209726	Amneal Pharmaceuticals NY LLC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE in 1 CARTON (69238-1422-6) / 160 TABLET, FILM COATED in 1 BOTTLE
69238-1422-8	69238-1422	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine	TABLET, FILM COATED	ORAL	20181023	N/A	ANDA	ANDA209726	Amneal Pharmaceuticals NY LLC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE in 1 CARTON (69238-1422-8) / 80 TABLET, FILM COATED in 1 BOTTLE
0363-0844-80	0363-0844	HUMAN OTC DRUG	All Night Pain Relief PM	Naproxen Sodium	TABLET	ORAL	20181231	N/A	ANDA	ANDA209726	Walgreens	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	80 TABLET in 1 BOTTLE, PLASTIC (0363-0844-80)
63868-411-20	63868-411	HUMAN OTC DRUG	Naproxen PM	Naproxen Sodium	TABLET	ORAL	20190131	20250601	ANDA	ANDA209726	QUALITY CHOICE (Chain Drug Marketing Association)	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE, PLASTIC in 1 BOX (63868-411-20) / 20 TABLET in 1 BOTTLE, PLASTIC