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=ANDA077614"
符合检索条件的记录共 147 条，共 8 页，当前第 6 页 ，可点击列名称排序
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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
68071-2230-9 68071-2230 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20200804 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 12.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2230-9)
68071-2780-6 68071-2780 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20240628 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 6.25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-2780-6)
68071-2780-8 68071-2780 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220705 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 6.25 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-2780-8)
68071-2780-9 68071-2780 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20220705 N/A ANDA ANDA077614 NuCare Pharmaceuticals,Inc. CARVEDILOL 6.25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2780-9)
68071-3138-3 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3138-3)
68071-3138-6 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3138-6)
68071-3138-8 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-3138-8)
68071-3138-9 68071-3138 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20170301 N/A ANDA ANDA077614 NuCare Pharmaceuticals, Inc. CARVEDILOL 3.125 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3138-9)
68084-854-01 68084-854 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20150504 N/A ANDA ANDA077614 American Health Packaging CARVEDILOL 6.25 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-854-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-854-11)
68382-092-01 68382-092 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 3.125 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-092-01)
68382-092-05 68382-092 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 3.125 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-092-05)
68382-092-17 68382-092 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 3.125 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68382-092-17)
68382-093-01 68382-093 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-093-01)
68382-093-05 68382-093 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-093-05)
68382-093-17 68382-093 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 6.25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68382-093-17)
68382-094-01 68382-094 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 12.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-094-01)
68382-094-05 68382-094 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 12.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-094-05)
68382-094-17 68382-094 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 12.5 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68382-094-17)
68382-095-01 68382-095 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-095-01)
68382-095-05 68382-095 HUMAN PRESCRIPTION DRUG Carvedilol Carvedilol TABLET, FILM COATED ORAL 20070905 N/A ANDA ANDA077614 Zydus Pharmaceuticals USA Inc. CARVEDILOL 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-095-05)
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