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=ANDA206923"
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
71335-1575-3 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20200513 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 60 TABLET in 1 BOTTLE (71335-1575-3)
71335-1575-4 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20200527 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (71335-1575-4)
71335-1575-5 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20260513 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 45 TABLET in 1 BOTTLE (71335-1575-5)
71335-1575-6 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20220321 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (71335-1575-6)
71335-1575-7 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20260513 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 25 TABLET in 1 BOTTLE (71335-1575-7)
71335-1575-8 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20260513 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 120 TABLET in 1 BOTTLE (71335-1575-8)
71335-1575-9 71335-1575 HUMAN PRESCRIPTION DRUG Trazodone Hydrochloride Trazodone Hydrochloride TABLET ORAL 20260513 N/A ANDA ANDA206923 Bryant Ranch Prepack TRAZODONE HYDROCHLORIDE 50 mg/1 28 TABLET in 1 BOTTLE (71335-1575-9)
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