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=ANDA078212"
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
50090-5751-2 50090-5751 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210930 N/A ANDA ANDA078212 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5751-2)
50090-5751-0 50090-5751 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210930 N/A ANDA ANDA078212 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5751-0)
84386-100-01 84386-100 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20260113 N/A ANDA ANDA078212 Aurobindo Pharma Limited BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (84386-100-01)
84386-100-90 84386-100 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20260113 N/A ANDA ANDA078212 Aurobindo Pharma Limited BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (84386-100-90)
84386-101-01 84386-101 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20260113 N/A ANDA ANDA078212 Aurobindo Pharma Limited BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (84386-101-01)
84386-101-90 84386-101 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20260113 N/A ANDA ANDA078212 Aurobindo Pharma Limited BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (84386-101-90)
84386-102-01 84386-102 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20260113 N/A ANDA ANDA078212 Aurobindo Pharma Limited BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (84386-102-01)
84386-102-90 84386-102 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20260113 N/A ANDA ANDA078212 Aurobindo Pharma Limited BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (84386-102-90)
50090-5750-1 50090-5750 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210930 N/A ANDA ANDA078212 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5750-1)
50090-5750-0 50090-5750 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210930 N/A ANDA ANDA078212 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5750-0)
71335-1365-1 71335-1365 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20200213 N/A ANDA ANDA078212 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1)
71335-1365-2 71335-1365 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20191007 N/A ANDA ANDA078212 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2)
71335-1365-3 71335-1365 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20240530 N/A ANDA ANDA078212 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3)
71335-1365-4 71335-1365 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20200311 N/A ANDA ANDA078212 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)
71205-320-30 71205-320 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA078212 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)
71205-320-60 71205-320 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA078212 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)
71205-320-90 71205-320 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA078212 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)
68788-7845-1 68788-7845 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210120 N/A ANDA ANDA078212 Preferred Pharmaceuticlas Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7845-1)
68788-7845-3 68788-7845 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210120 N/A ANDA ANDA078212 Preferred Pharmaceuticlas Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7845-3)
68788-7845-6 68788-7845 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, FILM COATED ORAL 20210120 N/A ANDA ANDA078212 Preferred Pharmaceuticlas Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7845-6)
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