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
70436-181-01	70436-181	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20220725	20241230	ANDA	ANDA215318	Slate Run Pharmaceuticals, LLC	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (70436-181-01)
70436-181-02	70436-181	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20220725	20241230	ANDA	ANDA215318	Slate Run Pharmaceuticals, LLC	IBUPROFEN	600 mg/1	500 TABLET in 1 BOTTLE (70436-181-02)
70436-180-01	70436-180	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20220725	20241230	ANDA	ANDA215318	Slate Run Pharmaceuticals, LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (70436-180-01)
70436-180-02	70436-180	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20220725	20241230	ANDA	ANDA215318	Slate Run Pharmaceuticals, LLC	IBUPROFEN	400 mg/1	500 TABLET in 1 BOTTLE (70436-180-02)
70436-182-01	70436-182	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20220725	20241230	ANDA	ANDA215318	Slate Run Pharmaceuticals, LLC	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (70436-182-01)
70436-182-02	70436-182	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20220725	20241230	ANDA	ANDA215318	Slate Run Pharmaceuticals, LLC	IBUPROFEN	800 mg/1	500 TABLET in 1 BOTTLE (70436-182-02)