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
76420-846-60	76420-846	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240908	N/A	ANDA	ANDA202413	Asclemed USA, Inc.	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-846-60)
11788-009-05	11788-009	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251215	N/A	ANDA	ANDA202413	AiPing Pharmaceutical, Inc.	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (11788-009-05)
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)
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)
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)
50090-7286-0	50090-7286	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241010	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (50090-7286-0)
71610-902-80	71610-902	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250501	N/A	ANDA	ANDA202413	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-902-80)
71610-902-92	71610-902	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250501	N/A	ANDA	ANDA202413	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	600 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71610-902-92)
67046-1606-3	67046-1606	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA202413	Coupler LLC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1606-3)
70518-4259-0	70518-4259	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250122	N/A	ANDA	ANDA202413	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4259-0)
70518-4259-1	70518-4259	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250122	N/A	ANDA	ANDA202413	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4259-1)
50090-7286-1	50090-7286	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (50090-7286-1)
50090-7286-4	50090-7286	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (50090-7286-4)
50090-7286-5	50090-7286	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241008	N/A	ANDA	ANDA202413	A-S Medication Solutions	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7286-5)
70512-794-90	70512-794	HUMAN PRESCRIPTION DRUG	Ibuprofen	ibuprofen	TABLET	ORAL	20250214	N/A	ANDA	ANDA202413	SOLA Pharmaceuticals, LLC	IBUPROFEN	300 mg/1	90 TABLET in 1 BOTTLE (70512-794-90)
69367-395-01	69367-395	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA202413	Westminster Pharmaceuticals, LLC	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69367-395-01)