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=NDA017442"
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
70518-3271-0 70518-3271 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride prazosin hydrochloride CAPSULE ORAL 20211117 N/A NDA AUTHORIZED GENERIC NDA017442 REMEDYREPACK INC. PRAZOSIN HYDROCHLORIDE 1 mg/1 30 POUCH in 1 BOX (70518-3271-0) / 1 CAPSULE in 1 POUCH (70518-3271-1)
66993-433-85 66993-433 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride prazosin hydrochloride CAPSULE ORAL 20220311 N/A NDA AUTHORIZED GENERIC NDA017442 Prasco Laboratories PRAZOSIN HYDROCHLORIDE 5 mg/1 90 CAPSULE in 1 BOTTLE (66993-433-85)
66993-432-85 66993-432 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride prazosin hydrochloride CAPSULE ORAL 20220311 N/A NDA AUTHORIZED GENERIC NDA017442 Prasco Laboratories PRAZOSIN HYDROCHLORIDE 2 mg/1 90 CAPSULE in 1 BOTTLE (66993-432-85)
66993-431-85 66993-431 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride prazosin hydrochloride CAPSULE ORAL 20210825 N/A NDA AUTHORIZED GENERIC NDA017442 Prasco Laboratories PRAZOSIN HYDROCHLORIDE 1 mg/1 90 CAPSULE in 1 BOTTLE (66993-431-85)
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