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=ANDA078861"
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
16714-601-02 16714-601 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride SOLUTION ORAL 20081031 N/A ANDA ANDA078861 NorthStar Rx LLC SERTRALINE HYDROCHLORIDE 20 mg/mL 1 BOTTLE, PLASTIC in 1 CARTON (16714-601-02) / 60 mL in 1 BOTTLE, PLASTIC
65862-224-20 65862-224 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride SOLUTION, CONCENTRATE ORAL 20081031 N/A ANDA ANDA078861 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 20 mg/mL 1 BOTTLE, PLASTIC in 1 CARTON (65862-224-20) / 60 mL in 1 BOTTLE, PLASTIC
65862-224-60 65862-224 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride SOLUTION, CONCENTRATE ORAL 20081031 N/A ANDA ANDA078861 Aurobindo Pharma Limited SERTRALINE HYDROCHLORIDE 20 mg/mL 1 BOTTLE in 1 CARTON (65862-224-60) / 60 mL in 1 BOTTLE
64980-409-06 64980-409 HUMAN PRESCRIPTION DRUG Sertraline Hydrochloride Sertraline Hydrochloride SOLUTION, CONCENTRATE ORAL 20081031 N/A ANDA ANDA078861 Rising Pharma Holdings, Inc. SERTRALINE HYDROCHLORIDE 20 mg/mL 1 BOTTLE, PLASTIC in 1 CARTON (64980-409-06) / 60 mL in 1 BOTTLE, PLASTIC
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