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=ANDA209293"
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
42858-703-03 42858-703 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180914 N/A ANDA ANDA209293 Rhodes Pharmaceuticals L.P. PAROXETINE HYDROCHLORIDE 12.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-703-03)
42858-703-50 42858-703 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180914 N/A ANDA ANDA209293 Rhodes Pharmaceuticals L.P. PAROXETINE HYDROCHLORIDE 12.5 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-703-50)
42858-705-03 42858-705 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180914 N/A ANDA ANDA209293 Rhodes Pharmaceuticals L.P. PAROXETINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-705-03)
42858-705-50 42858-705 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180914 N/A ANDA ANDA209293 Rhodes Pharmaceuticals L.P. PAROXETINE HYDROCHLORIDE 25 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-705-50)
42858-707-03 42858-707 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180914 N/A ANDA ANDA209293 Rhodes Pharmaceuticals L.P. PAROXETINE HYDROCHLORIDE 37.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-707-03)
42858-707-50 42858-707 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180914 N/A ANDA ANDA209293 Rhodes Pharmaceuticals L.P. PAROXETINE HYDROCHLORIDE 37.5 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42858-707-50)
63629-9498-1 63629-9498 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221214 N/A ANDA ANDA209293 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 12.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9498-1)
63629-9499-1 63629-9499 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221214 N/A ANDA ANDA209293 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9499-1)
63629-9500-1 63629-9500 HUMAN PRESCRIPTION DRUG PAROXETINE PAROXETINE HYDROCHLORIDE HEMIHYDRATE TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221214 N/A ANDA ANDA209293 Bryant Ranch Prepack PAROXETINE HYDROCHLORIDE HEMIHYDRATE 37.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9500-1)
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