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
0121-1038-40	0121-1038	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20251017	N/A	ANDA	ANDA077404	PAI Holdings, LLC dba PAI Pharma	MEGESTROL ACETATE	400 mg/10mL	4 TRAY in 1 CASE (0121-1038-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1038-10)
0121-1038-00	0121-1038	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20251017	N/A	ANDA	ANDA077404	PAI Holdings, LLC dba PAI Pharma	MEGESTROL ACETATE	400 mg/10mL	10 TRAY in 1 CASE (0121-1038-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1038-10)
70954-896-20	70954-896	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20240702	N/A	ANDA	ANDA077404	ANI Pharmaceuticals, Inc.	MEGESTROL ACETATE	40 mg/mL	480 mL in 1 BOTTLE (70954-896-20)
70954-896-10	70954-896	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20240702	N/A	ANDA	ANDA077404	ANI Pharmaceuticals, Inc.	MEGESTROL ACETATE	40 mg/mL	240 mL in 1 BOTTLE (70954-896-10)