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=ANDA213349"
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
27241-181-30 27241-181 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (27241-181-30)
27241-181-90 27241-181 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (27241-181-90)
27241-182-30 27241-182 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (27241-182-30)
27241-182-90 27241-182 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (27241-182-90)
27241-180-30 27241-180 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (27241-180-30)
27241-180-90 27241-180 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (27241-180-90)
27241-179-30 27241-179 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220331 N/A ANDA ANDA213349 Ajanta Pharma USA Inc. NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (27241-179-30)
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