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=ANDA075520"
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
51672-4002-6 51672-4002 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20000508 N/A ANDA ANDA075520 Taro Pharmaceuticals U.S.A., Inc. NORTRIPTYLINE HYDROCHLORIDE 25 mg/1 30 CAPSULE in 1 BOTTLE (51672-4002-6)
60760-401-30 60760-401 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20171215 N/A ANDA ANDA075520 St. Mary's Medical Park Pharmacy NORTRIPTYLINE HYDROCHLORIDE 50 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-401-30)
50090-0537-0 50090-0537 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20160629 N/A ANDA ANDA075520 A-S Medication Solutions NORTRIPTYLINE HYDROCHLORIDE 10 mg/1 60 CAPSULE in 1 BOTTLE (50090-0537-0)
50090-0537-1 50090-0537 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20160629 N/A ANDA ANDA075520 A-S Medication Solutions NORTRIPTYLINE HYDROCHLORIDE 10 mg/1 30 CAPSULE in 1 BOTTLE (50090-0537-1)
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