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=ANDA202239"
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
68788-8454-3 68788-8454 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20230602 N/A ANDA ANDA202239 Preferred Pharmaceuticals Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 30 CAPSULE in 1 BOTTLE (68788-8454-3)
57237-147-01 57237-147 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 40 mg/1 100 CAPSULE in 1 BOTTLE (57237-147-01)
57237-147-05 57237-147 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 40 mg/1 500 CAPSULE in 1 BOTTLE (57237-147-05)
42291-015-01 42291-015 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20230620 N/A ANDA ANDA202239 AvKARE AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 40 mg/1 100 CAPSULE in 1 BOTTLE (42291-015-01)
50090-1042-0 50090-1042 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20141128 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 5 mg/1; 20 mg/1 30 CAPSULE in 1 BOTTLE (50090-1042-0)
50090-1042-1 50090-1042 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20141128 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 5 mg/1; 20 mg/1 90 CAPSULE in 1 BOTTLE (50090-1042-1)
50090-7361-0 50090-7361 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20241017 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 30 CAPSULE in 1 BOTTLE (50090-7361-0)
50090-7361-1 50090-7361 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20241017 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 90 CAPSULE in 1 BOTTLE (50090-7361-1)
70518-1928-0 70518-1928 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20190301 N/A ANDA ANDA202239 REMEDYREPACK INC. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 5 mg/1; 10 mg/1 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-1928-0)
57237-146-01 57237-146 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 100 CAPSULE in 1 BOTTLE (57237-146-01)
57237-146-05 57237-146 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 500 CAPSULE in 1 BOTTLE (57237-146-05)
42291-014-01 42291-014 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20230620 N/A ANDA ANDA202239 AvKARE AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 100 CAPSULE in 1 BOTTLE (42291-014-01)
50090-3357-0 50090-3357 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20180131 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 5 mg/1; 40 mg/1 90 CAPSULE in 1 BOTTLE (50090-3357-0)
50090-1418-0 50090-1418 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20141128 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 30 CAPSULE in 1 BOTTLE (50090-1418-0)
50090-1418-1 50090-1418 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20141128 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 90 CAPSULE in 1 BOTTLE (50090-1418-1)
72789-412-90 72789-412 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20240606 N/A ANDA ANDA202239 PD-Rx Pharmaceuticals, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 20 mg/1 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-412-90)
50090-2720-0 50090-2720 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20161220 N/A ANDA ANDA202239 A-S Medication Solutions AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 10 mg/1; 40 mg/1 90 CAPSULE in 1 BOTTLE (50090-2720-0)
57237-144-01 57237-144 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 5 mg/1; 20 mg/1 100 CAPSULE in 1 BOTTLE (57237-144-01)
57237-142-01 57237-142 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 2.5 mg/1; 10 mg/1 100 CAPSULE in 1 BOTTLE (57237-142-01)
57237-142-05 57237-142 HUMAN PRESCRIPTION DRUG Amlodipine and Benazepril Hydrochloride Amlodipine and Benazepril Hydrochloride CAPSULE ORAL 20120905 N/A ANDA ANDA202239 Rising Pharma Holdings, Inc. AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 2.5 mg/1; 10 mg/1 500 CAPSULE in 1 BOTTLE (57237-142-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase