美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 078466 007 ANDA AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE CAPSULE; ORAL 10MG; 40MG No 2010/02/05 LUPIN PHARMS Prescription
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 078466 007 ANDA AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE CAPSULE; ORAL 10MG; 40MG No 2011/07/05 LUPIN PHARMS Prescription
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 078652 001 ANDA AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE CAPSULE; ORAL 2.5MG; 10MG No 2013/03/28 (TA) ZYDUS PHARMS USA INC None (Tentative Approval)
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 078652 002 ANDA AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE CAPSULE; ORAL 5MG; 10MG No 2013/03/28 (TA) ZYDUS PHARMS USA INC None (Tentative Approval)
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 078652 003 ANDA AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE CAPSULE; ORAL 5MG; 20MG No 2013/03/28 (TA) ZYDUS PHARMS USA INC None (Tentative Approval)
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE 078652 004 ANDA AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE CAPSULE; ORAL 10MG; 20MG No 2013/03/28 (TA) ZYDUS PHARMS USA INC None (Tentative Approval)
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