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=ANDA202389"
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
51655-149-52 51655-149 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20210507 N/A ANDA ANDA202389 Northwind Health Company, LLC ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-52)
16729-170-01 16729-170 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20130321 N/A ANDA ANDA202389 Accord Healthcare Inc. ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16729-170-01)
16729-168-01 16729-168 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20130305 N/A ANDA ANDA202389 Accord Healthcare Inc. ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16729-168-01)
16729-168-17 16729-168 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20140723 N/A ANDA ANDA202389 Accord Healthcare Inc. ESCITALOPRAM OXALATE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16729-168-17)
16729-170-17 16729-170 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20131112 N/A ANDA ANDA202389 Accord Healthcare Inc. ESCITALOPRAM OXALATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)
16729-169-01 16729-169 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20130319 N/A ANDA ANDA202389 Accord Healthcare Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16729-169-01)
16729-169-17 16729-169 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20131112 N/A ANDA ANDA202389 Accord Healthcare Inc. ESCITALOPRAM OXALATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16729-169-17)
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