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=ANDA213052"
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
59651-271-01 59651-271 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride Prazosin Hydrochloride CAPSULE ORAL 20230331 N/A ANDA ANDA213052 Aurobindo Pharma Limited PRAZOSIN HYDROCHLORIDE 1 mg/1 100 CAPSULE in 1 BOTTLE (59651-271-01)
59651-271-99 59651-271 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride Prazosin Hydrochloride CAPSULE ORAL 20230331 N/A ANDA ANDA213052 Aurobindo Pharma Limited PRAZOSIN HYDROCHLORIDE 1 mg/1 1000 CAPSULE in 1 BOTTLE (59651-271-99)
59651-272-01 59651-272 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride Prazosin Hydrochloride CAPSULE ORAL 20230331 N/A ANDA ANDA213052 Aurobindo Pharma Limited PRAZOSIN HYDROCHLORIDE 2 mg/1 100 CAPSULE in 1 BOTTLE (59651-272-01)
59651-272-99 59651-272 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride Prazosin Hydrochloride CAPSULE ORAL 20230331 N/A ANDA ANDA213052 Aurobindo Pharma Limited PRAZOSIN HYDROCHLORIDE 2 mg/1 1000 CAPSULE in 1 BOTTLE (59651-272-99)
59651-273-01 59651-273 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride Prazosin Hydrochloride CAPSULE ORAL 20230331 N/A ANDA ANDA213052 Aurobindo Pharma Limited PRAZOSIN HYDROCHLORIDE 5 mg/1 100 CAPSULE in 1 BOTTLE (59651-273-01)
59651-273-25 59651-273 HUMAN PRESCRIPTION DRUG Prazosin Hydrochloride Prazosin Hydrochloride CAPSULE ORAL 20230331 N/A ANDA ANDA213052 Aurobindo Pharma Limited PRAZOSIN HYDROCHLORIDE 5 mg/1 250 CAPSULE in 1 BOTTLE (59651-273-25)
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