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=ANDA211364"
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
71205-910-30 71205-910 HUMAN PRESCRIPTION DRUG Clomipramine Hydrochloride Clomipramine Hydrochloride CAPSULE ORAL 20210716 N/A ANDA ANDA211364 Proficient Rx LP CLOMIPRAMINE HYDROCHLORIDE 25 mg/1 30 CAPSULE in 1 BOTTLE (71205-910-30)
71205-910-55 71205-910 HUMAN PRESCRIPTION DRUG Clomipramine Hydrochloride Clomipramine Hydrochloride CAPSULE ORAL 20210716 N/A ANDA ANDA211364 Proficient Rx LP CLOMIPRAMINE HYDROCHLORIDE 25 mg/1 500 CAPSULE in 1 BOTTLE (71205-910-55)
71205-912-30 71205-912 HUMAN PRESCRIPTION DRUG Clomipramine Hydrochloride Clomipramine Hydrochloride CAPSULE ORAL 20210716 N/A ANDA ANDA211364 Proficient Rx LP CLOMIPRAMINE HYDROCHLORIDE 75 mg/1 30 CAPSULE in 1 BOTTLE (71205-912-30)
71205-912-55 71205-912 HUMAN PRESCRIPTION DRUG Clomipramine Hydrochloride Clomipramine Hydrochloride CAPSULE ORAL 20210716 N/A ANDA ANDA211364 Proficient Rx LP CLOMIPRAMINE HYDROCHLORIDE 75 mg/1 500 CAPSULE in 1 BOTTLE (71205-912-55)
71205-912-60 71205-912 HUMAN PRESCRIPTION DRUG Clomipramine Hydrochloride Clomipramine Hydrochloride CAPSULE ORAL 20210716 N/A ANDA ANDA211364 Proficient Rx LP CLOMIPRAMINE HYDROCHLORIDE 75 mg/1 60 CAPSULE in 1 BOTTLE (71205-912-60)
71205-912-90 71205-912 HUMAN PRESCRIPTION DRUG Clomipramine Hydrochloride Clomipramine Hydrochloride CAPSULE ORAL 20210716 N/A ANDA ANDA211364 Proficient Rx LP CLOMIPRAMINE HYDROCHLORIDE 75 mg/1 90 CAPSULE in 1 BOTTLE (71205-912-90)
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