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
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)
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)
62135-400-12	62135-400	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220810	N/A	ANDA	ANDA202413	Chartwell RX, LLC	IBUPROFEN	400 mg/1	120 TABLET, FILM COATED in 1 PACKAGE (62135-400-12)
85509-2396-6	85509-2396	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250730	N/A	ANDA	ANDA202413	PHOENIX RX LLC	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85509-2396-6)
85509-2396-3	85509-2396	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250730	N/A	ANDA	ANDA202413	PHOENIX RX LLC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85509-2396-3)
85509-2396-9	85509-2396	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250730	N/A	ANDA	ANDA202413	PHOENIX RX LLC	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85509-2396-9)
82804-227-60	82804-227	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250812	N/A	ANDA	ANDA202413	Proficient Rx LP	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-227-60)
82804-227-90	82804-227	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250903	N/A	ANDA	ANDA202413	Proficient Rx LP	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-227-90)
82804-227-30	82804-227	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250714	N/A	ANDA	ANDA202413	Proficient Rx LP	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-227-30)
68788-4039-5	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (68788-4039-5)
68788-4039-6	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-4039-6)
68788-4039-8	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68788-4039-8)
68788-4039-9	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-4039-9)
68788-4039-2	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-4039-2)
68788-4039-3	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-4039-3)
68788-4039-1	68788-4039	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-4039-1)
50090-7281-7	50090-7281	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-7281-7)
50090-7282-0	50090-7282	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7282-0)
50090-7281-5	50090-7281	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7281-5)
50090-7283-1	50090-7283	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (50090-7283-1)