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=ANDA208717"
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
71209-059-04 71209-059 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (71209-059-04)
71209-059-05 71209-059 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (71209-059-05)
71209-059-11 71209-059 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 5 mg/1 1000 TABLET in 1 BOTTLE (71209-059-11)
72241-032-04 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (72241-032-04)
72241-032-05 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (72241-032-05)
72241-032-11 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 1000 TABLET in 1 BOTTLE (72241-032-11)
72241-032-22 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (72241-032-22)
72162-2417-3 72162-2417 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20241031 N/A ANDA ANDA208717 Bryant Ranch Prepack NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (72162-2417-3)
72162-2417-9 72162-2417 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20241031 N/A ANDA ANDA208717 Bryant Ranch Prepack NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (72162-2417-9)
72162-2414-3 72162-2414 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20241031 N/A ANDA ANDA208717 Bryant Ranch Prepack NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (72162-2414-3)
72162-2414-9 72162-2414 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20241031 N/A ANDA ANDA208717 Bryant Ranch Prepack NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (72162-2414-9)
71209-060-01 71209-060 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (71209-060-01)
71209-060-04 71209-060 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (71209-060-04)
71209-060-05 71209-060 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (71209-060-05)
71209-060-11 71209-060 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (71209-060-11)
72241-033-04 72241-033 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (72241-033-04)
72241-033-05 72241-033 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (72241-033-05)
72241-033-11 72241-033 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 1000 TABLET in 1 BOTTLE (72241-033-11)
72241-033-22 72241-033 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (72241-033-22)
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