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
76420-848-30	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)
82804-137-15	82804-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241001	N/A	ANDA	ANDA202413	Proficient Rx LP	IBUPROFEN	400 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (82804-137-15)
82804-137-30	82804-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20241024	N/A	ANDA	ANDA202413	Proficient Rx LP	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-137-30)
82804-137-60	82804-137	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20240830	N/A	ANDA	ANDA202413	Proficient Rx LP	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-137-60)