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=ANDA074132"
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
63629-3204-4 63629-3204 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20211222 N/A ANDA ANDA074132 Bryant Ranch Prepack NORTRIPTYLINE HYDROCHLORIDE 10 mg/1 100 CAPSULE in 1 BOTTLE (63629-3204-4)
63629-3204-5 63629-3204 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20110510 N/A ANDA ANDA074132 Bryant Ranch Prepack NORTRIPTYLINE HYDROCHLORIDE 10 mg/1 120 CAPSULE in 1 BOTTLE (63629-3204-5)
63629-3204-6 63629-3204 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20140613 N/A ANDA ANDA074132 Bryant Ranch Prepack NORTRIPTYLINE HYDROCHLORIDE 10 mg/1 15 CAPSULE in 1 BOTTLE (63629-3204-6)
71335-0065-3 71335-0065 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20211227 N/A ANDA ANDA074132 Bryant Ranch Prepack NORTRIPTYLINE HYDROCHLORIDE 75 mg/1 90 CAPSULE in 1 BOTTLE (71335-0065-3)
71335-0065-4 71335-0065 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20211227 N/A ANDA ANDA074132 Bryant Ranch Prepack NORTRIPTYLINE HYDROCHLORIDE 75 mg/1 28 CAPSULE in 1 BOTTLE (71335-0065-4)
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