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
0116-4021-41	0116-4021	HUMAN PRESCRIPTION DRUG	Valproic Acid	Valproic Acid	SOLUTION	ORAL	20250729	N/A	ANDA	ANDA070868	Xttrium Laboratories Inc.	VALPROIC ACID	250 mg/5mL	10 TRAY in 1 CASE (0116-4021-41) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05)
0116-4021-40	0116-4021	HUMAN PRESCRIPTION DRUG	Valproic Acid	Valproic Acid	SOLUTION	ORAL	20250729	N/A	ANDA	ANDA070868	Xttrium Laboratories Inc.	VALPROIC ACID	250 mg/5mL	4 TRAY in 1 CASE (0116-4021-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05)
0116-4021-16	0116-4021	HUMAN PRESCRIPTION DRUG	Valproic Acid	Valproic Acid	SOLUTION	ORAL	20250729	N/A	ANDA	ANDA070868	Xttrium Laboratories Inc.	VALPROIC ACID	250 mg/5mL	473 mL in 1 BOTTLE, PLASTIC (0116-4021-16)
0116-4021-11	0116-4021	HUMAN PRESCRIPTION DRUG	Valproic Acid	Valproic Acid	SOLUTION	ORAL	20250729	N/A	ANDA	ANDA070868	Xttrium Laboratories Inc.	VALPROIC ACID	250 mg/5mL	10 TRAY in 1 CASE (0116-4021-11) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4021-10)