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
72189-339-60	72189-339	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20220405	N/A	ANDA	ANDA077794	DirectRx	OXCARBAZEPINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-339-60)
0615-8153-39	0615-8153	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20190611	20240430	ANDA	ANDA077794	NCS HealthCare of KY, LLC dba Vangard Labs	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8153-39)
62756-183-08	62756-183	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-183-08)
62756-183-13	62756-183	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62756-183-13)
62756-183-18	62756-183	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-183-18)
62756-183-83	62756-183	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-183-83)
62756-183-88	62756-183	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-183-88)
62756-184-08	62756-184	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-184-08)
62756-184-13	62756-184	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62756-184-13)
62756-184-18	62756-184	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-184-18)
62756-184-83	62756-184	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-184-83)
62756-184-88	62756-184	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-184-88)
62756-185-08	62756-185	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-185-08)
62756-185-13	62756-185	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62756-185-13)
62756-185-18	62756-185	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	600 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-185-18)
62756-185-83	62756-185	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-185-83)
62756-185-88	62756-185	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077794	Sun Pharmaceutical Industries, Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-185-88)
70518-1027-0	70518-1027	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20180220	N/A	ANDA	ANDA077794	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1027-0)
70518-1027-1	70518-1027	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20210818	N/A	ANDA	ANDA077794	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-1027-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1027-2)
70518-1027-3	70518-1027	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20210920	N/A	ANDA	ANDA077794	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-1027-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1027-4)