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
0363-9766-08	0363-9766	HUMAN OTC DRUG	Naproxen Sodium Diphenhydramine HCl	Naproxen Sodium Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210619	20250930	ANDA	ANDA213663	WALGREEN CO.	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	80 TABLET, FILM COATED in 1 BOTTLE (0363-9766-08)
79903-204-20	79903-204	HUMAN OTC DRUG	Naproxen Sodium Diphenhydramine HCL	Naproxen Sodium Diphenhydramine HCL	TABLET	ORAL	20231214	N/A	ANDA	ANDA213663	Walmart	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	20 TABLET in 1 BOTTLE (79903-204-20)
21130-814-05	21130-814	HUMAN OTC DRUG	Naproxen Sodium Diphenhydramine Hydrochloride	Naproxen Sodium Diphenhydramine Hydrochloride	TABLET	ORAL	20230630	N/A	ANDA	ANDA213663	SAFEWAY	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	50 TABLET in 1 BOTTLE (21130-814-05)
11673-819-08	11673-819	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCL	Naproxen Sodium and Diphenhydramine HCL	TABLET	ORAL	20240301	N/A	ANDA	ANDA213663	TARGET CORPORATION	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	80 TABLET in 1 BOTTLE (11673-819-08)
69842-328-02	69842-328	HUMAN OTC DRUG	Naproxen Sodium Diphenhydramine HCl	Naproxen Sodium Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210514	N/A	ANDA	ANDA213663	CVS PHARMACY, INC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (69842-328-02)
69842-328-08	69842-328	HUMAN OTC DRUG	Naproxen Sodium Diphenhydramine HCl	Naproxen Sodium Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210514	20250228	ANDA	ANDA213663	CVS PHARMACY, INC	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	80 TABLET, FILM COATED in 1 BOTTLE (69842-328-08)
62207-814-38	62207-814	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210220	N/A	ANDA	ANDA213663	Granules India Ltd	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	37500 TABLET, FILM COATED in 1 POUCH (62207-814-38)
62207-814-39	62207-814	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210220	N/A	ANDA	ANDA213663	Granules India Ltd	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	7500 TABLET, FILM COATED in 1 POUCH (62207-814-39)
62207-814-47	62207-814	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210220	N/A	ANDA	ANDA213663	Granules India Ltd	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62207-814-47)
62207-814-95	62207-814	HUMAN OTC DRUG	Naproxen Sodium and Diphenhydramine HCl	Naproxen Sodium and Diphenhydramine HCl	TABLET, FILM COATED	ORAL	20210220	N/A	ANDA	ANDA213663	Granules India Ltd	DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM	25 mg/1; 220 mg/1	1 BOTTLE in 1 CARTON (62207-814-95) / 20 TABLET, FILM COATED in 1 BOTTLE