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
17856-0907-1	17856-0907	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20240510	N/A	ANDA	ANDA075671	ATLANTIC BIOLOGICALS CORP.	MEGESTROL ACETATE	40 mg/mL	48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0907-1) / 10 mL in 1 SYRINGE
17856-0907-2	17856-0907	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20240510	N/A	ANDA	ANDA075671	ATLANTIC BIOLOGICALS CORP.	MEGESTROL ACETATE	40 mg/mL	20 mL in 1 CUP (17856-0907-2)
17856-0907-3	17856-0907	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20240510	N/A	ANDA	ANDA075671	ATLANTIC BIOLOGICALS CORP.	MEGESTROL ACETATE	40 mg/mL	10 mL in 1 CUP (17856-0907-3)
17856-0907-5	17856-0907	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20240510	N/A	ANDA	ANDA075671	ATLANTIC BIOLOGICALS CORP.	MEGESTROL ACETATE	40 mg/mL	5 mL in 1 SYRINGE (17856-0907-5)
66689-020-50	66689-020	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20120822	20250331	ANDA	ANDA075671	VistaPharm, LLC	MEGESTROL ACETATE	40 mg/mL	5 TRAY in 1 CASE (66689-020-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (66689-020-01)
66689-020-99	66689-020	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20120822	20250331	ANDA	ANDA075671	VistaPharm, LLC	MEGESTROL ACETATE	40 mg/mL	10 TRAY in 1 CASE (66689-020-99) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (66689-020-01)
63739-549-73	63739-549	HUMAN PRESCRIPTION DRUG	Megestrol Acetate	Megestrol Acetate	SUSPENSION	ORAL	20231218	N/A	ANDA	ANDA075671	McKesson Corporation dba SKY Packaging	MEGESTROL ACETATE	400 mg/10mL	40 CUP, UNIT-DOSE in 1 CASE (63739-549-73) / 10 mL in 1 CUP, UNIT-DOSE (63739-549-72)