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=ANDA077069"
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
63629-2001-1 63629-2001 HUMAN PRESCRIPTION DRUG Amiodarone HCl Amiodarone Hydrochloride TABLET ORAL 20220208 N/A ANDA ANDA077069 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 400 mg/1 30 TABLET in 1 BOTTLE (63629-2001-1)
63629-2076-1 63629-2076 HUMAN PRESCRIPTION DRUG Amiodarone HCl Amiodarone Hydrochloride TABLET ORAL 20220208 N/A ANDA ANDA077069 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (63629-2076-1)
62135-576-30 62135-576 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20230817 N/A ANDA ANDA077069 Chartwell RX, LLC AMIODARONE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (62135-576-30)
62135-577-60 62135-577 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20230817 N/A ANDA ANDA077069 Chartwell RX, LLC AMIODARONE HYDROCHLORIDE 200 mg/1 60 TABLET in 1 BOTTLE (62135-577-60)
62135-578-30 62135-578 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20230817 N/A ANDA ANDA077069 Chartwell RX, LLC AMIODARONE HYDROCHLORIDE 400 mg/1 30 TABLET in 1 BOTTLE (62135-578-30)
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