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
68788-8757-4	68788-8757	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241017	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	800 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68788-8757-4)
68788-8757-5	68788-8757	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241017	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	800 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (68788-8757-5)
68788-8757-6	68788-8757	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241017	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8757-6)
50090-7288-5	50090-7288	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50090-7288-5)
50090-7288-7	50090-7288	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (50090-7288-7)
68071-3679-1	68071-3679	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240904	N/A	ANDA	ANDA202413	NuCare Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-3679-1)
73614-201-03	73614-201	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250210	N/A	ANDA	ANDA202413	Brisk Pharmaceuticals	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (73614-201-03)
76420-847-01	76420-847	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-847-01)
76420-847-05	76420-847	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-847-05)
76420-847-30	76420-847	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-847-30)
50090-7288-8	50090-7288	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-7288-8)
50090-7288-9	50090-7288	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	24 TABLET, FILM COATED in 1 BOTTLE (50090-7288-9)
68788-8754-2	68788-8754	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-8754-2)
68788-8754-3	68788-8754	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8754-3)
76420-848-01	76420-848	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-848-01)
76420-848-05	76420-848	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-848-05)
76420-848-30	76420-848	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-848-30)
76420-848-60	76420-848	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-848-60)
76420-848-90	76420-848	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-848-90)
68788-8754-4	68788-8754	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	600 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68788-8754-4)