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
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)
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)
70518-2902-1	70518-2902	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260423	N/A	ANDA	ANDA202413	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	50 POUCH in 1 BOX (70518-2902-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2902-2)
67296-2184-3	67296-2184	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA202413	Redpharm Drug	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-2184-3)
62135-402-12	62135-402	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220810	N/A	ANDA	ANDA202413	Chartwell RX, LLC	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 PACKAGE (62135-402-12)
68071-3793-1	68071-3793	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250407	N/A	ANDA	ANDA202413	NuCare Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (68071-3793-1)
68071-3793-3	68071-3793	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250213	N/A	ANDA	ANDA202413	NuCare Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3793-3)
68071-3793-5	68071-3793	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250311	N/A	ANDA	ANDA202413	NuCare Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-3793-5)
68071-3793-6	68071-3793	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250213	N/A	ANDA	ANDA202413	NuCare Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-3793-6)
68071-3849-4	68071-3849	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250514	N/A	ANDA	ANDA202413	NuCare Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (68071-3849-4)
62135-401-12	62135-401	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220810	N/A	ANDA	ANDA202413	Chartwell RX, LLC	IBUPROFEN	600 mg/1	120 TABLET, FILM COATED in 1 PACKAGE (62135-401-12)
71335-3121-6	71335-3121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260413	N/A	ANDA	ANDA202413	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-3121-6)
71335-3121-7	71335-3121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260413	N/A	ANDA	ANDA202413	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-3121-7)
71335-3121-8	71335-3121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260413	N/A	ANDA	ANDA202413	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-3121-8)
71335-3121-9	71335-3121	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260413	N/A	ANDA	ANDA202413	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-3121-9)