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)
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)
70518-1027-5	70518-1027	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20231209	N/A	ANDA	ANDA077794	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1027-5)
63629-4987-1	63629-4987	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20140214	N/A	ANDA	ANDA077794	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-4987-1)
63629-4987-2	63629-4987	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20130418	N/A	ANDA	ANDA077794	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-4987-2)
63629-4987-3	63629-4987	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20140121	N/A	ANDA	ANDA077794	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-4987-3)
63629-4987-4	63629-4987	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240402	N/A	ANDA	ANDA077794	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (63629-4987-4)
63629-4987-5	63629-4987	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240402	N/A	ANDA	ANDA077794	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (63629-4987-5)
70518-1842-3	70518-1842	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230107	N/A	ANDA	ANDA077794	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	100 POUCH in 1 BOX (70518-1842-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1842-4)
70518-1842-5	70518-1842	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20230612	N/A	ANDA	ANDA077794	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1842-5)
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)