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=ANDA078216"
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
13668-010-06 13668-010 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20071018 N/A ANDA ANDA078216 Torrent Pharmaceuticals Limited CITALOPRAM HYDROBROMIDE 20 mg/1 5600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06)
13668-010-30 13668-010 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20071018 N/A ANDA ANDA078216 Torrent Pharmaceuticals Limited CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)
60760-495-30 60760-495 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20250529 N/A ANDA ANDA078216 St Marys Medical Park Pharmacy CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-495-30)
43063-481-05 43063-481 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20150403 N/A ANDA ANDA078216 PD-Rx Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-05)
43063-481-30 43063-481 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20161027 N/A ANDA ANDA078216 PD-Rx Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-30)
43063-683-60 43063-683 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20170915 N/A ANDA ANDA078216 PD-Rx Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-60)
43063-683-90 43063-683 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20161025 N/A ANDA ANDA078216 PD-Rx Pharmaceuticals, Inc. CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-90)
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