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
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)
51655-065-26 51655-065 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220527 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-065-26)
51655-065-52 51655-065 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20160623 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (51655-065-52)
71335-0267-1 71335-0267 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (71335-0267-1)
71335-0267-2 71335-0267 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (71335-0267-2)
71335-0267-3 71335-0267 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, COATED in 1 BOTTLE (71335-0267-3)
68071-5130-0 68071-5130 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20191212 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 100 TABLET, COATED in 1 BOTTLE (68071-5130-0)
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)
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)
68071-3324-1 68071-3324 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170710 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 120 TABLET, COATED in 1 BOTTLE (68071-3324-1)
68071-3324-3 68071-3324 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170710 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-3324-3)
68071-3324-6 68071-3324 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170710 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 60 TABLET, COATED in 1 BOTTLE (68071-3324-6)
71335-0267-4 71335-0267 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (71335-0267-4)
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