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
0121-0675-85	0121-0675	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20210811	N/A	ANDA	ANDA075379	PAI Holdings, LLC	VALPROIC ACID	250 mg/5mL	473 mL in 1 BOTTLE (0121-0675-85)
0121-0675-16	0121-0675	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20050411	N/A	ANDA	ANDA075379	PAI Holdings, LLC	VALPROIC ACID	250 mg/5mL	473 mL in 1 BOTTLE (0121-0675-16)
71335-2250-1	71335-2250	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20240129	N/A	ANDA	ANDA075379	Bryant Ranch Prepack	VALPROIC ACID	250 mg/5mL	473 mL in 1 BOTTLE (71335-2250-1)
0121-1350-00	0121-1350	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20050411	N/A	ANDA	ANDA075379	PAI Holdings, LLC	VALPROIC ACID	500 mg/10mL	10 TRAY in 1 CASE (0121-1350-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1350-10)
70518-3805-0	70518-3805	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20230725	N/A	ANDA	ANDA075379	REMEDYREPACK INC.	VALPROIC ACID	250 mg/5mL	10 CUP, UNIT-DOSE in 1 BOX (70518-3805-0) / 5 mL in 1 CUP, UNIT-DOSE (70518-3805-1)
70518-3805-2	70518-3805	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20240313	N/A	ANDA	ANDA075379	REMEDYREPACK INC.	VALPROIC ACID	250 mg/5mL	10 CUP, UNIT-DOSE in 1 BOX (70518-3805-2) / 10 mL in 1 CUP, UNIT-DOSE (70518-3805-3)
0121-4675-40	0121-4675	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20050411	N/A	ANDA	ANDA075379	PAI Holdings, LLC	VALPROIC ACID	250 mg/5mL	4 TRAY in 1 CASE (0121-4675-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4675-05)
0121-4675-00	0121-4675	HUMAN PRESCRIPTION DRUG	VALPROIC ACID	VALPROIC ACID	SOLUTION	ORAL	20050411	N/A	ANDA	ANDA075379	PAI Holdings, LLC	VALPROIC ACID	250 mg/5mL	10 TRAY in 1 CASE (0121-4675-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4675-05)