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=ANDA217411"
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
16571-105-01 16571-105 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20230610 N/A ANDA ANDA217411 Rising Pharma Holdings, Inc. AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (16571-105-01)
16571-105-10 16571-105 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20230610 N/A ANDA ANDA217411 Rising Pharma Holdings, Inc. AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (16571-105-10)
16571-109-01 16571-109 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20230610 N/A ANDA ANDA217411 Rising Pharma Holdings, Inc. AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (16571-109-01)
71335-2491-4 71335-2491 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20240916 N/A ANDA ANDA217411 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (71335-2491-4)
71335-2491-5 71335-2491 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20240916 N/A ANDA ANDA217411 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 20 TABLET in 1 BOTTLE (71335-2491-5)
71335-2491-6 71335-2491 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20240916 N/A ANDA ANDA217411 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 28 TABLET in 1 BOTTLE (71335-2491-6)
71335-2491-7 71335-2491 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20240916 N/A ANDA ANDA217411 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 56 TABLET in 1 BOTTLE (71335-2491-7)
71335-2491-8 71335-2491 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET ORAL 20240916 N/A ANDA ANDA217411 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 180 TABLET in 1 BOTTLE (71335-2491-8)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase