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=ANDA203828"
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
50090-5752-0 50090-5752 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210930 N/A ANDA ANDA203828 A-S Medication Solutions NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (50090-5752-0)
50090-5752-1 50090-5752 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20210930 N/A ANDA ANDA203828 A-S Medication Solutions NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (50090-5752-1)
60687-641-21 60687-641 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220907 N/A ANDA ANDA203828 American Health Packaging NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 BLISTER PACK in 1 CARTON (60687-641-21) / 1 TABLET in 1 BLISTER PACK (60687-641-11)
60687-652-21 60687-652 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20220907 N/A ANDA ANDA203828 American Health Packaging NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 BLISTER PACK in 1 CARTON (60687-652-21) / 1 TABLET in 1 BLISTER PACK (60687-652-11)
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