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
10267-5062-4 10267-5062 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210124 N/A ANDA ANDA213474 Contract Pharmacal Corp. DOXEPIN HYDROCHLORIDE 75 mg/1 1000 CAPSULE in 1 BOTTLE (10267-5062-4)
10267-5062-9 10267-5062 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20210124 N/A ANDA ANDA213474 Contract Pharmacal Corp. DOXEPIN HYDROCHLORIDE 75 mg/1 90 CAPSULE in 1 BOTTLE (10267-5062-9)
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)
71335-2408-1 71335-2408 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20240918 N/A ANDA ANDA213474 Bryant Ranch Prepack DOXEPIN HYDROCHLORIDE 50 mg/1 60 CAPSULE in 1 BOTTLE (71335-2408-1)
71335-2408-2 71335-2408 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20240918 N/A ANDA ANDA213474 Bryant Ranch Prepack DOXEPIN HYDROCHLORIDE 50 mg/1 30 CAPSULE in 1 BOTTLE (71335-2408-2)
71335-2408-3 71335-2408 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20240918 N/A ANDA ANDA213474 Bryant Ranch Prepack DOXEPIN HYDROCHLORIDE 50 mg/1 90 CAPSULE in 1 BOTTLE (71335-2408-3)
71335-2408-4 71335-2408 HUMAN PRESCRIPTION DRUG Doxepin Hydrochloride Doxepin Hydrochloride CAPSULE ORAL 20240918 N/A ANDA ANDA213474 Bryant Ranch Prepack DOXEPIN HYDROCHLORIDE 50 mg/1 120 CAPSULE in 1 BOTTLE (71335-2408-4)
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