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
68196-601-60	68196-601	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20240615	N/A	ANDA	ANDA091239	SAM'S WEST INC	IBUPROFEN	200 mg/1	600 TABLET, COATED in 1 BOTTLE (68196-601-60)
68210-0800-1	68210-0800	HUMAN OTC DRUG	VALUMEDS IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170519	N/A	ANDA	ANDA091239	SPIRIT PHARMACEUTICALS LLC	IBUPROFEN	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68210-0800-1)
68210-0800-4	68210-0800	HUMAN OTC DRUG	VALUMEDS IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180411	N/A	ANDA	ANDA091239	SPIRIT PHARMACEUTICALS LLC	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (68210-0800-4) / 40 TABLET, FILM COATED in 1 BOTTLE
0363-9600-42	0363-9600	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	24 TABLET in 1 BOTTLE, PLASTIC (0363-9600-42)
0363-9600-50	0363-9600	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (0363-9600-50)
0363-9601-01	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0363-9601-01)
0363-9601-05	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	50 TABLET in 1 BOTTLE, PLASTIC (0363-9601-05)
0363-9601-10	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0363-9601-10)
0363-9601-15	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	150 TABLET in 1 BOTTLE, PLASTIC (0363-9601-15)
0363-9601-20	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20251001	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	200 TABLET in 1 BOTTLE, PLASTIC (0363-9601-20)
0363-9601-42	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	24 TABLET in 1 BOTTLE, PLASTIC (0363-9601-42)
0363-9601-50	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (0363-9601-50)
0363-9601-97	0363-9601	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20181211	N/A	ANDA	ANDA091239	WALGREENS	IBUPROFEN	200 mg/1	2 BOTTLE in 1 CARTON (0363-9601-97) / 100 TABLET in 1 BOTTLE
11673-990-20	11673-990	HUMAN OTC DRUG	IBUPROFEN CA	IBUPROFEN	TABLET, COATED	ORAL	20200101	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	200 TABLET, COATED in 1 BOTTLE (11673-990-20)
11673-990-42	11673-990	HUMAN OTC DRUG	IBUPROFEN CA	IBUPROFEN	TABLET, COATED	ORAL	20200101	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	24 TABLET, COATED in 1 BOTTLE (11673-990-42)
11673-991-01	11673-991	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200204	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	100 TABLET, COATED in 1 BOTTLE (11673-991-01)
11673-991-05	11673-991	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200204	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	50 TABLET, COATED in 1 BOTTLE (11673-991-05)
11673-991-20	11673-991	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200204	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	200 TABLET, COATED in 1 BOTTLE (11673-991-20)
11673-991-50	11673-991	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200204	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	500 TABLET, COATED in 1 BOTTLE (11673-991-50)
11673-991-88	11673-991	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200204	N/A	ANDA	ANDA091239	TARGET CORPORATION	IBUPROFEN	200 mg/1	1000 TABLET, COATED in 1 BOTTLE (11673-991-88)