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
70518-2254-0	70518-2254	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190805	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2254-0)
70518-2276-0	70518-2276	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190822	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2276-0)
70518-2253-1	70518-2253	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20210803	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	100 POUCH in 1 BOX (70518-2253-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2253-2)
70518-2377-2	70518-2377	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20210805	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-2377-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2377-3)
70518-2253-0	70518-2253	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20190805	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2253-0)
70518-2377-0	70518-2377	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20191023	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-2377-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2377-1)
70518-2370-2	70518-2370	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20241004	N/A	ANDA	ANDA078069	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	100 POUCH in 1 BOX (70518-2370-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2370-3)
51991-054-01	51991-054	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-054-01)
51991-055-01	51991-055	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-055-01)
51991-055-05	51991-055	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-055-05)
51991-054-05	51991-054	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-054-05)
51991-053-01	51991-053	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-053-01)
51991-053-05	51991-053	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20250129	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-053-05)
51991-292-01	51991-292	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-292-01)
51991-294-01	51991-294	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-294-01)
51991-294-05	51991-294	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-294-05)
51991-292-05	51991-292	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-292-05)
51991-293-01	51991-293	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51991-293-01)
51991-293-05	51991-293	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Breckenridge Pharmaceutical, Inc.	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)
63629-2075-1	63629-2075	HUMAN PRESCRIPTION DRUG	OXCARBAZEPINE	OXCARBAZEPINE	TABLET, FILM COATED	ORAL	20080111	N/A	ANDA	ANDA078069	Bryant Ranch Prepack	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63629-2075-1)