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
71335-0078-4 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE (71335-0078-4)
71335-0078-5 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 14 TABLET, COATED in 1 BOTTLE (71335-0078-5)
71335-0078-6 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 10 TABLET, COATED in 1 BOTTLE (71335-0078-6)
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)
63187-499-90 63187-499 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150202 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE (63187-499-90)
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)
51407-463-01 51407-463 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET, COATED in 1 BOTTLE (51407-463-01)
51407-463-05 51407-463 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 500 TABLET, COATED in 1 BOTTLE (51407-463-05)
50090-3775-0 50090-3775 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20181105 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (50090-3775-0)
50090-3775-2 50090-3775 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20181105 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE (50090-3775-2)
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)
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