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=ANDA076118"
符合检索条件的记录共 93 条，共 5 页，当前第 2 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
43547-338-03 43547-338 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20190630 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (43547-338-03)
43547-338-10 43547-338 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (43547-338-10)
43547-338-50 43547-338 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 40 mg/1 500 TABLET, COATED in 1 BOTTLE (43547-338-50)
68788-6889-1 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 100 TABLET, COATED in 1 BOTTLE (68788-6889-1)
68788-6889-3 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 30 TABLET, COATED in 1 BOTTLE (68788-6889-3)
68788-6889-6 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 60 TABLET, COATED in 1 BOTTLE (68788-6889-6)
68788-6889-8 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 120 TABLET, COATED in 1 BOTTLE (68788-6889-8)
68788-6889-9 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 90 TABLET, COATED in 1 BOTTLE (68788-6889-9)
68788-6957-1 68788-6957 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170502 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (68788-6957-1)
68788-6957-3 68788-6957 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170502 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (68788-6957-3)
68788-6957-6 68788-6957 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170502 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, COATED in 1 BOTTLE (68788-6957-6)
68788-6957-8 68788-6957 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170502 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 120 TABLET, COATED in 1 BOTTLE (68788-6957-8)
68788-6957-9 68788-6957 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170502 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (68788-6957-9)
50090-0914-0 50090-0914 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20141128 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (50090-0914-0)
50090-0914-1 50090-0914 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20141128 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (50090-0914-1)
68071-1769-1 68071-1769 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20191018 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (68071-1769-1)
68071-1770-1 68071-1770 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170802 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (68071-1770-1)
68071-1969-2 68071-1969 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20180702 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 120 TABLET, COATED in 1 BOTTLE (68071-1969-2)
68071-1969-3 68071-1969 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20180702 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-1969-3)
68071-1969-6 68071-1969 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20180702 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 60 TABLET, COATED in 1 BOTTLE (68071-1969-6)
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