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
43063-867-01	43063-867	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180711	N/A	ANDA	ANDA090796	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-01)
43063-867-10	43063-867	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180905	N/A	ANDA	ANDA090796	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-10)
43063-867-30	43063-867	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20231030	N/A	ANDA	ANDA090796	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-30)
43063-867-60	43063-867	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180705	N/A	ANDA	ANDA090796	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-60)
80425-0089-1	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1)
80425-0089-2	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2)
80425-0089-3	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (80425-0089-3)
80425-0089-4	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4)
67296-1756-1	67296-1756	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200101	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	800 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (67296-1756-1)
42708-097-30	42708-097	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA090796	QPharma Inc	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42708-097-30)
68071-4459-6	68071-4459	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
67296-1685-2	67296-1685	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (67296-1685-2)
67296-1685-3	67296-1685	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	RedPharm Drug, Inc.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1685-3)
73086-210-01	73086-210	HUMAN PRESCRIPTION DRUG	ibuprofen	ibuprofen	TABLET	ORAL	20240320	N/A	ANDA	ANDA090796	SKYA HEALTH, LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (73086-210-01)
49483-603-01	49483-603	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-603-01)
49483-603-03	49483-603	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (49483-603-03)
49483-603-05	49483-603	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-603-05)
49483-603-50	49483-603	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (49483-603-50)
68071-4243-1	68071-4243	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180122	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-4243-1)
71335-1503-0	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)