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
68788-8322-4	68788-8322	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20230123	N/A	ANDA	ANDA076925	Preferred Pharmaceuticals Inc.	IBUPROFEN	100 mg/5mL	473 mL in 1 BOTTLE (68788-8322-4)
71205-716-72	71205-716	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20221114	N/A	ANDA	ANDA076925	Proficient Rx LP	IBUPROFEN	100 mg/5mL	1 BOTTLE in 1 CARTON (71205-716-72) / 120 mL in 1 BOTTLE
81033-018-52	81033-018	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20250101	N/A	ANDA	ANDA076925	Kesin Pharma Corporation	IBUPROFEN	100 mg/5mL	100 CUP, UNIT-DOSE in 1 CASE (81033-018-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-018-10)
81033-018-50	81033-018	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20250101	N/A	ANDA	ANDA076925	Kesin Pharma Corporation	IBUPROFEN	100 mg/5mL	100 CUP, UNIT-DOSE in 1 CASE (81033-018-50) / 5 mL in 1 CUP, UNIT-DOSE (81033-018-05)
59368-402-01	59368-402	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20041228	N/A	ANDA	ANDA076925	Praxis, LLC	IBUPROFEN	100 mg/5mL	1 BOTTLE in 1 CARTON (59368-402-01) / 120 mL in 1 BOTTLE
45802-952-26	45802-952	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20041228	N/A	ANDA	ANDA076925	Padagis Israel Pharmaceuticals Ltd	IBUPROFEN	100 mg/5mL	1 BOTTLE in 1 CARTON (45802-952-26) / 120 mL in 1 BOTTLE
45802-952-43	45802-952	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	SUSPENSION	ORAL	20041208	N/A	ANDA	ANDA076925	Padagis Israel Pharmaceuticals Ltd	IBUPROFEN	100 mg/5mL	473 mL in 1 BOTTLE (45802-952-43)