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=ANDA078032"
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
68788-7461-6 68788-7461 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078032 Preferred Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7461-6)
68788-7461-8 68788-7461 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078032 Preferred Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 20 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68788-7461-8)
68788-7461-9 68788-7461 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078032 Preferred Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7461-9)
55700-818-30 55700-818 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20191114 20260717 ANDA ANDA078032 Quality Care Products, LLC ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55700-818-30)
55700-818-90 55700-818 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20191114 20260720 ANDA ANDA078032 Quality Care Products, LLC ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (55700-818-90)
50090-5312-0 50090-5312 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20201029 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5312-0)
71335-1307-1 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20200206 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1307-1)
71335-1307-2 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-1307-2)
71335-1307-3 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1307-3)
71335-1307-4 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20190920 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1307-4)
71335-1307-5 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20200629 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1307-5)
71335-1307-6 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20200827 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1307-6)
71335-1307-7 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-1307-7)
71335-1307-8 71335-1307 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230126 N/A ANDA ANDA078032 Bryant Ranch Prepack ESCITALOPRAM OXALATE 20 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-1307-8)
60687-865-01 60687-865 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20250320 N/A ANDA ANDA078032 American Health Packaging ESCITALOPRAM OXALATE 5 mg/1 100 BLISTER PACK in 1 CARTON (60687-865-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-865-11)
50090-5312-1 50090-5312 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230713 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5312-1)
50090-6534-0 50090-6534 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230628 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0)
50090-6534-1 50090-6534 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230628 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6534-1)
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