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=ANDA212661"
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
72603-872-01 72603-872 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (72603-872-01)
72603-872-02 72603-872 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (72603-872-02)
33342-458-07 33342-458 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (33342-458-07)
33342-458-10 33342-458 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (33342-458-10)
33342-458-25 33342-458 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 5 mg/1 12 BLISTER PACK in 1 CARTON (33342-458-25) / 10 TABLET in 1 BLISTER PACK
72603-870-01 72603-870 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (72603-870-01)
33342-460-07 33342-460 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (33342-460-07)
33342-460-10 33342-460 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (33342-460-10)
33342-460-25 33342-460 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 12 BLISTER PACK in 1 CARTON (33342-460-25) / 10 TABLET in 1 BLISTER PACK
72603-873-01 72603-873 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (72603-873-01)
72603-873-02 72603-873 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (72603-873-02)
33342-459-07 33342-459 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (33342-459-07)
33342-459-10 33342-459 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (33342-459-10)
33342-459-25 33342-459 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 10 mg/1 12 BLISTER PACK in 1 CARTON (33342-459-25) / 10 TABLET in 1 BLISTER PACK
72603-871-01 72603-871 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BOTTLE (72603-871-01)
72603-871-02 72603-871 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250714 N/A ANDA ANDA212661 NorthStar RxLLC NEBIVOLOL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (72603-871-02)
33342-457-07 33342-457 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (33342-457-07)
33342-457-10 33342-457 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (33342-457-10)
33342-457-25 33342-457 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20250129 N/A ANDA ANDA212661 Macleods Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 12 BLISTER PACK in 1 CARTON (33342-457-25) / 10 TABLET in 1 BLISTER PACK
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