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=ANDA077137"
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
69097-731-07 69097-731 HUMAN PRESCRIPTION DRUG TERBINAFINE HYDROCHLORIDE Terbinafine Tablets 250 mg TABLET ORAL 20210108 N/A ANDA ANDA077137 Cipla USA Inc. TERBINAFINE HYDROCHLORIDE 250 mg/1 100 TABLET in 1 BOTTLE (69097-731-07)
69097-731-02 69097-731 HUMAN PRESCRIPTION DRUG TERBINAFINE HYDROCHLORIDE Terbinafine Tablets 250 mg TABLET ORAL 20210108 N/A ANDA ANDA077137 Cipla USA Inc. TERBINAFINE HYDROCHLORIDE 250 mg/1 30 TABLET in 1 BOTTLE (69097-731-02)
63187-792-35 63187-792 HUMAN PRESCRIPTION DRUG Terbinafine Hydrochloride Terbinafine Hydrochloride TABLET ORAL 20170801 N/A ANDA ANDA077137 Proficient Rx LP TERBINAFINE HYDROCHLORIDE 250 mg/1 35 TABLET in 1 BOTTLE (63187-792-35)
63187-792-90 63187-792 HUMAN PRESCRIPTION DRUG Terbinafine Hydrochloride Terbinafine Hydrochloride TABLET ORAL 20170102 N/A ANDA ANDA077137 Proficient Rx LP TERBINAFINE HYDROCHLORIDE 250 mg/1 90 TABLET in 1 BOTTLE (63187-792-90)
63187-792-30 63187-792 HUMAN PRESCRIPTION DRUG Terbinafine Hydrochloride Terbinafine Hydrochloride TABLET ORAL 20170102 N/A ANDA ANDA077137 Proficient Rx LP TERBINAFINE HYDROCHLORIDE 250 mg/1 30 TABLET in 1 BOTTLE (63187-792-30)
63187-792-45 63187-792 HUMAN PRESCRIPTION DRUG Terbinafine Hydrochloride Terbinafine Hydrochloride TABLET ORAL 20170703 N/A ANDA ANDA077137 Proficient Rx LP TERBINAFINE HYDROCHLORIDE 250 mg/1 45 TABLET in 1 BOTTLE (63187-792-45)
63187-792-60 63187-792 HUMAN PRESCRIPTION DRUG Terbinafine Hydrochloride Terbinafine Hydrochloride TABLET ORAL 20170102 N/A ANDA ANDA077137 Proficient Rx LP TERBINAFINE HYDROCHLORIDE 250 mg/1 60 TABLET in 1 BOTTLE (63187-792-60)
68071-1640-3 68071-1640 HUMAN PRESCRIPTION DRUG Terbinafine Hydrochloride Terbinafine Hydrochloride TABLET ORAL 20171102 N/A ANDA ANDA077137 NuCare Pharmaceuticals,Inc. TERBINAFINE HYDROCHLORIDE 250 mg/1 30 TABLET in 1 BOTTLE (68071-1640-3)
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