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=ANDA213406"
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
70377-067-11 70377-067 HUMAN PRESCRIPTION DRUG Prazosin hydrochloride Prazosin hydrochloride CAPSULE ORAL 20230109 N/A ANDA ANDA213406 Biocon Pharma Inc. PRAZOSIN HYDROCHLORIDE 2 mg/1 100 CAPSULE in 1 BOTTLE (70377-067-11)
70377-068-11 70377-068 HUMAN PRESCRIPTION DRUG Prazosin hydrochloride Prazosin hydrochloride CAPSULE ORAL 20230109 N/A ANDA ANDA213406 Biocon Pharma Inc. PRAZOSIN HYDROCHLORIDE 5 mg/1 100 CAPSULE in 1 BOTTLE (70377-068-11)
70518-3928-0 70518-3928 HUMAN PRESCRIPTION DRUG Prazosin hydrochloride Prazosin hydrochloride CAPSULE ORAL 20231129 N/A ANDA ANDA213406 REMEDYREPACK INC. PRAZOSIN HYDROCHLORIDE 1 mg/1 30 CAPSULE in 1 BLISTER PACK (70518-3928-0)
70377-066-11 70377-066 HUMAN PRESCRIPTION DRUG Prazosin hydrochloride Prazosin hydrochloride CAPSULE ORAL 20230109 N/A ANDA ANDA213406 Biocon Pharma Inc. PRAZOSIN HYDROCHLORIDE 1 mg/1 100 CAPSULE in 1 BOTTLE (70377-066-11)
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