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
55910-768-24	55910-768	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20170430	20261230	ANDA	ANDA079174	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	IBUPROFEN	200 mg/1	1 BOTTLE, PLASTIC in 1 BOX (55910-768-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
0924-0076-00	0924-0076	HUMAN OTC DRUG	Physicians Care Ibuprofen	Ibuprofen 200mg	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA079174	Acme United Corporation	IBUPROFEN	200 mg/1	2 TABLET, FILM COATED in 1 PACKET (0924-0076-00)
0924-0076-01	0924-0076	HUMAN OTC DRUG	Physicians Care Ibuprofen	Ibuprofen 200mg	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA079174	Acme United Corporation	IBUPROFEN	200 mg/1	50 PACKET in 1 CARTON (0924-0076-01) / 2 TABLET, FILM COATED in 1 PACKET (0924-0076-00)
0924-0076-02	0924-0076	HUMAN OTC DRUG	Physicians Care Ibuprofen	Ibuprofen 200mg	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA079174	Acme United Corporation	IBUPROFEN	200 mg/1	125 PACKET in 1 CARTON (0924-0076-02) / 2 TABLET, FILM COATED in 1 PACKET
0363-9594-07	0363-9594	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20230901	N/A	ANDA	ANDA079174	WALGREENS CO.	IBUPROFEN	200 mg/1	15 TABLET in 1 BOTTLE (0363-9594-07)
0363-9594-10	0363-9594	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET	ORAL	20211015	N/A	ANDA	ANDA079174	WALGREENS CO.	IBUPROFEN	200 mg/1	100 TABLET in 1 BOTTLE (0363-9594-10)
55910-847-02	55910-847	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20200312	N/A	ANDA	ANDA079174	Dolgencorp, Inc.	IBUPROFEN	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (55910-847-02)
37808-109-03	37808-109	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20101201	N/A	ANDA	ANDA079174	HEB	IBUPROFEN	200 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (37808-109-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
37808-109-08	37808-109	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20130301	N/A	ANDA	ANDA079174	HEB	IBUPROFEN	200 mg/1	250 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-109-08)
37808-109-10	37808-109	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20101201	N/A	ANDA	ANDA079174	HEB	IBUPROFEN	200 mg/1	2 BOTTLE, PLASTIC in 1 CARTON (37808-109-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
55910-847-10	55910-847	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20200312	N/A	ANDA	ANDA079174	Dolgencorp, Inc.	IBUPROFEN	200 mg/1	2 BOTTLE in 1 CARTON (55910-847-10) / 100 TABLET, FILM COATED in 1 BOTTLE
69729-157-10	69729-157	HUMAN OTC DRUG	Ibuwin Forte	Ibuprofen	TABLET	ORAL	20231229	N/A	ANDA	ANDA079174	OPMX LLC	IBUPROFEN	200 mg/1	1 BLISTER PACK in 1 CARTON (69729-157-10) / 10 TABLET in 1 BLISTER PACK
37835-581-01	37835-581	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250201	N/A	ANDA	ANDA079174	Bi-Mart	IBUPROFEN	200 mg/1	100 TABLET in 1 BOTTLE (37835-581-01)
37835-581-05	37835-581	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250201	N/A	ANDA	ANDA079174	Bi-Mart	IBUPROFEN	200 mg/1	500 TABLET in 1 BOTTLE (37835-581-05)
37835-581-10	37835-581	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250201	N/A	ANDA	ANDA079174	Bi-Mart	IBUPROFEN	200 mg/1	1000 TABLET in 1 BOTTLE (37835-581-10)
37835-581-25	37835-581	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250201	N/A	ANDA	ANDA079174	Bi-Mart	IBUPROFEN	200 mg/1	250 TABLET in 1 BOTTLE (37835-581-25)
37835-585-25	37835-585	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250201	N/A	ANDA	ANDA079174	BI-MART	IBUPROFEN	200 mg/1	250 TABLET in 1 BOTTLE (37835-585-25)
41163-509-06	41163-509	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20181231	N/A	ANDA	ANDA079174	United Natural Foods, Inc. dba UNFI	IBUPROFEN	200 mg/1	1000 TABLET, COATED in 1 BOTTLE, PLASTIC (41163-509-06)
41163-509-17	41163-509	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20181231	N/A	ANDA	ANDA079174	United Natural Foods, Inc. dba UNFI	IBUPROFEN	200 mg/1	150 TABLET, COATED in 1 BOTTLE, PLASTIC (41163-509-17)
42507-909-22	42507-909	HUMAN OTC DRUG	Ibuprofen	Ibuprofen	TABLET, COATED	ORAL	20260113	N/A	ANDA	ANDA079174	HYVEE INC	IBUPROFEN	200 mg/1	200 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-909-22)