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=ANDA216172"
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
70756-025-30 70756-025 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (70756-025-30)
70756-291-30 70756-291 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (70756-291-30)
70756-291-90 70756-291 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (70756-291-90)
70756-292-30 70756-292 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (70756-292-30)
70756-292-90 70756-292 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (70756-292-90)
70756-293-30 70756-293 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (70756-293-30)
70756-293-90 70756-293 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20221114 N/A ANDA ANDA216172 Lifestar Pharma LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (70756-293-90)
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