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
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)
51407-464-01 51407-464 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (51407-464-01)
51407-464-05 51407-464 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 500 TABLET, COATED in 1 BOTTLE (51407-464-05)
51407-465-01 51407-465 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (51407-465-01)
51407-465-05 51407-465 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 500 TABLET, COATED in 1 BOTTLE (51407-465-05)
72189-110-30 72189-110 HUMAN PRESCRIPTION DRUG BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE TABLET, COATED ORAL 20200612 N/A ANDA ANDA076118 DIRECT RX BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (72189-110-30)
72189-110-90 72189-110 HUMAN PRESCRIPTION DRUG BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE TABLET, COATED ORAL 20200612 N/A ANDA ANDA076118 DIRECT RX BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE (72189-110-90)
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)
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)
70518-2125-0 70518-2125 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20190531 N/A ANDA ANDA076118 REMEDYREPACK INC. BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2125-0)
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)
51655-066-26 51655-066 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220711 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)
51655-066-52 51655-066 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20160304 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)
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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase