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=ANDA213474"
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
72162-2227-1 72162-2227 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20240126 N/A ANDA ANDA213474 Bryant Ranch Prepack DOXEPIN HYDROCHLORIDE 25 mg/1 100 CAPSULE in 1 BOTTLE (72162-2227-1)
72162-2228-1 72162-2228 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20240126 N/A ANDA ANDA213474 Bryant Ranch Prepack DOXEPIN HYDROCHLORIDE 75 mg/1 100 CAPSULE in 1 BOTTLE (72162-2228-1)
71921-162-01 71921-162 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210501 N/A ANDA ANDA213474 Florida Pharmaceutical Products, LLC DOXEPIN HYDROCHLORIDE 10 mg/1 100 CAPSULE in 1 BOTTLE (71921-162-01)
71921-163-01 71921-163 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210501 N/A ANDA ANDA213474 Florida Pharmaceutical Products, LLC DOXEPIN HYDROCHLORIDE 25 mg/1 100 CAPSULE in 1 BOTTLE (71921-163-01)
71921-164-01 71921-164 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210501 N/A ANDA ANDA213474 Florida Pharmaceutical Products, LLC DOXEPIN HYDROCHLORIDE 50 mg/1 100 CAPSULE in 1 BOTTLE (71921-164-01)
71921-165-01 71921-165 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210501 N/A ANDA ANDA213474 Florida Pharmaceutical Products, LLC DOXEPIN HYDROCHLORIDE 75 mg/1 100 CAPSULE in 1 BOTTLE (71921-165-01)
71921-166-01 71921-166 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210501 N/A ANDA ANDA213474 Florida Pharmaceutical Products, LLC DOXEPIN HYDROCHLORIDE 100 mg/1 100 CAPSULE in 1 BOTTLE (71921-166-01)
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