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)
检索条件:" 注册申请号=ANDA090939"
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
0904-6427-61 0904-6427 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20141015 N/A ANDA ANDA090939 Major Pharmaceuticals ESCITALOPRAM OXALATE 20 mg/1 100 BLISTER PACK in 1 CARTON (0904-6427-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
82009-035-10 82009-035 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET ORAL 20230301 N/A ANDA ANDA090939 Quallent Pharmaceuticals Health LLC ESCITALOPRAM OXALATE 5 mg/1 1000 TABLET in 1 BOTTLE (82009-035-10)
71205-792-30 71205-792 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET ORAL 20230418 N/A ANDA ANDA090939 Proficient Rx LP ESCITALOPRAM OXALATE 10 mg/1 30 TABLET in 1 BOTTLE (71205-792-30)
71205-792-60 71205-792 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET ORAL 20230418 N/A ANDA ANDA090939 Proficient Rx LP ESCITALOPRAM OXALATE 10 mg/1 60 TABLET in 1 BOTTLE (71205-792-60)
71205-792-90 71205-792 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET ORAL 20230418 N/A ANDA ANDA090939 Proficient Rx LP ESCITALOPRAM OXALATE 10 mg/1 90 TABLET in 1 BOTTLE (71205-792-90)
13668-137-01 13668-137 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Torrent Pharmaceuticals Limited ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13668-137-01)
13668-137-05 13668-137 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Torrent Pharmaceuticals Limited ESCITALOPRAM OXALATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13668-137-05)
13668-137-10 13668-137 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Torrent Pharmaceuticals Limited ESCITALOPRAM OXALATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13668-137-10)
13668-137-20 13668-137 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Torrent Pharmaceuticals Limited ESCITALOPRAM OXALATE 20 mg/1 2000 TABLET, FILM COATED in 1 BOTTLE (13668-137-20)
13668-137-30 13668-137 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Torrent Pharmaceuticals Limited ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-137-30)
68788-8371-1 68788-8371 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20230201 N/A ANDA ANDA090939 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8371-1)
68788-8371-3 68788-8371 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20230201 N/A ANDA ANDA090939 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8371-3)
68788-8371-6 68788-8371 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20230201 N/A ANDA ANDA090939 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8371-6)
68788-8371-8 68788-8371 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20230201 N/A ANDA ANDA090939 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68788-8371-8)
68788-8371-9 68788-8371 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20230201 N/A ANDA ANDA090939 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8371-9)
55154-6893-0 55154-6893 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20141015 N/A ANDA ANDA090939 Cardinal Health 107, LLC ESCITALOPRAM OXALATE 10 mg/1 10 BLISTER PACK in 1 BAG (55154-6893-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
82009-036-10 82009-036 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET ORAL 20230301 N/A ANDA ANDA090939 Quallent Pharmaceuticals Health LLC ESCITALOPRAM OXALATE 10 mg/1 1000 TABLET in 1 BOTTLE (82009-036-10)
82982-065-60 82982-065 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET ORAL 20230501 20260731 ANDA ANDA090939 Pharmasource Meds, LLC ESCITALOPRAM OXALATE 10 mg/1 60 TABLET in 1 BOTTLE (82982-065-60)
72162-2241-0 72162-2241 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Bryant Ranch Prepack ESCITALOPRAM OXALATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2241-0)
72162-2241-1 72162-2241 HUMAN PRESCRIPTION DRUG escitalopram oxalate escitalopram oxalate TABLET, FILM COATED ORAL 20120911 N/A ANDA ANDA090939 Bryant Ranch Prepack ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2241-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase