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=ANDA211444"
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
80426-044-01 80426-044 HUMAN PRESCRIPTION DRUG FLUOXETINE FLUOXETINE TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA211444 PEL HEALTHCARE LLC FLUOXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80426-044-01)
80426-044-02 80426-044 HUMAN PRESCRIPTION DRUG FLUOXETINE FLUOXETINE TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA211444 PEL HEALTHCARE LLC FLUOXETINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80426-044-02)
80426-045-02 80426-045 HUMAN PRESCRIPTION DRUG FLUOXETINE FLUOXETINE TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA211444 PEL HEALTHCARE LLC FLUOXETINE HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80426-045-02)
80426-045-01 80426-045 HUMAN PRESCRIPTION DRUG FLUOXETINE FLUOXETINE TABLET, FILM COATED ORAL 20230313 N/A ANDA ANDA211444 PEL HEALTHCARE LLC FLUOXETINE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80426-045-01)
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