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
51655-116-52 51655-116 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220711 N/A ANDA ANDA078032 Northwind Pharmaceuticals, LLC ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-52)
42708-155-30 42708-155 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220804 N/A ANDA ANDA078032 QPharma Inc ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-155-30)
42708-163-30 42708-163 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA078032 QPharma Inc ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-163-30)
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)
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)
50090-6190-0 50090-6190 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20221028 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6190-0)
50090-6190-1 50090-6190 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20221028 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6190-1)
50090-6191-0 50090-6191 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20221028 N/A ANDA ANDA078032 A-S Medication Solutions ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6191-0)
51655-277-26 51655-277 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20221005 N/A ANDA ANDA078032 Northwind Pharmaceuticals, LLC ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-26)
51655-277-52 51655-277 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220908 N/A ANDA ANDA078032 Northwind Pharmaceuticals, LLC ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52)
51655-284-26 51655-284 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20200513 N/A ANDA ANDA078032 Northwind Pharmaceuticals ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-26)
51655-284-52 51655-284 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220720 N/A ANDA ANDA078032 Northwind Pharmaceuticals ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-52)
53002-2438-0 53002-2438 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220501 N/A ANDA ANDA078032 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (53002-2438-0)
53002-2438-3 53002-2438 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220501 N/A ANDA ANDA078032 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-2438-3)
53002-2438-6 53002-2438 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20220501 N/A ANDA ANDA078032 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (53002-2438-6)
53002-5453-0 53002-5453 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230101 N/A ANDA ANDA078032 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (53002-5453-0)
53002-5453-3 53002-5453 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230101 N/A ANDA ANDA078032 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-5453-3)
53002-5453-6 53002-5453 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20230101 N/A ANDA ANDA078032 RPK Pharmaceuticals, Inc. ESCITALOPRAM OXALATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (53002-5453-6)
55700-818-30 55700-818 HUMAN PRESCRIPTION DRUG Escitalopram Escitalopram TABLET, FILM COATED ORAL 20191114 N/A 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 N/A ANDA ANDA078032 Quality Care Products, LLC ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (55700-818-90)
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