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"
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
68071-1769-1 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)
43547-335-03 43547-335 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20190630 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 5 mg/1 30 TABLET, COATED in 1 BOTTLE (43547-335-03)
43547-335-10 43547-335 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 5 mg/1 100 TABLET, COATED in 1 BOTTLE (43547-335-10)
50090-3243-0 50090-3243 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20171117 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE (50090-3243-0)
50090-3243-1 50090-3243 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20171103 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE (50090-3243-1)
63187-906-30 63187-906 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170901 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (63187-906-30)
63187-906-60 63187-906 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170901 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, COATED in 1 BOTTLE (63187-906-60)
63187-906-90 63187-906 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170901 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (63187-906-90)
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)
43547-337-03 43547-337 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20190630 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE (43547-337-03)
43547-337-10 43547-337 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (43547-337-10)
43547-337-50 43547-337 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 500 TABLET, COATED in 1 BOTTLE (43547-337-50)
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)
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)
43547-336-03 43547-336 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20190630 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (43547-336-03)
43547-336-10 43547-336 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET, COATED in 1 BOTTLE (43547-336-10)
43547-336-50 43547-336 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20140101 N/A ANDA ANDA076118 Solco healthcare U.S., LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 500 TABLET, COATED in 1 BOTTLE (43547-336-50)
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