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
70518-3237-2	70518-3237	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20250211	N/A	ANDA	ANDA077802	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3237-2)
70518-3237-0	70518-3237	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20211013	N/A	ANDA	ANDA077802	REMEDYREPACK INC.	OXCARBAZEPINE	300 mg/1	100 POUCH in 1 BOX (70518-3237-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3237-1)
70518-3197-1	70518-3197	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA077802	REMEDYREPACK INC.	OXCARBAZEPINE	600 mg/1	100 POUCH in 1 BOX (70518-3197-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3197-2)
72189-573-60	72189-573	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20240909	N/A	ANDA	ANDA077802	Direct_rx	OXCARBAZEPINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-573-60)
68462-138-05	68462-138	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077802	Glenmark Pharmaceuticals Inc., USA	OXCARBAZEPINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-138-05)
68462-139-01	68462-139	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077802	Glenmark Pharmaceuticals Inc., USA	OXCARBAZEPINE	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-139-01)
68462-139-05	68462-139	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077802	Glenmark Pharmaceuticals Inc., USA	OXCARBAZEPINE	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-139-05)
68462-137-01	68462-137	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077802	Glenmark Pharmaceuticals Inc., USA	OXCARBAZEPINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-137-01)
68462-137-05	68462-137	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077802	Glenmark Pharmaceuticals Inc., USA	OXCARBAZEPINE	150 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-137-05)
68462-138-01	68462-138	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20071009	N/A	ANDA	ANDA077802	Glenmark Pharmaceuticals Inc., USA	OXCARBAZEPINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-138-01)
67046-1073-3	67046-1073	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20241111	N/A	ANDA	ANDA077802	Coupler LLC	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1073-3)
71205-411-30	71205-411	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20200226	N/A	ANDA	ANDA077802	Proficient Rx LP	OXCARBAZEPINE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-411-30)
71205-411-60	71205-411	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20200226	N/A	ANDA	ANDA077802	Proficient Rx LP	OXCARBAZEPINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-411-60)
71205-411-90	71205-411	HUMAN PRESCRIPTION DRUG	Oxcarbazepine	Oxcarbazepine	TABLET, FILM COATED	ORAL	20200226	N/A	ANDA	ANDA077802	Proficient Rx LP	OXCARBAZEPINE	150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-411-90)