Overview
Moexipril is a non-sulfhydryl containing precursor of the active angiotensin-converting enzyme (ACE) inhibitor moexiprilat. It is used to treat high blood pressure (hypertension). It works by relaxing blood vessels, causing them to widen. Lowering high blood pressure helps prevent strokes, heart attacks and kidney problems.
Background
Moexipril is a non-sulfhydryl containing precursor of the active angiotensin-converting enzyme (ACE) inhibitor moexiprilat. It is used to treat high blood pressure (hypertension). It works by relaxing blood vessels, causing them to widen. Lowering high blood pressure helps prevent strokes, heart attacks and kidney problems.
Indication
用于治疗高血压。
Associated Conditions
- Hypertension
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2009/10/09 | Phase 1 | Completed | |||
2009/10/06 | Phase 1 | Completed | |||
2009/02/03 | Phase 1 | Completed | |||
2009/02/03 | Phase 1 | Completed | |||
2008/01/08 | Phase 2 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Physicians Total Care, Inc. | 54868-5928 | ORAL | 7.5 mg in 1 1 | 4/14/2011 | |
| UCB, Inc. | 0091-3707 | ORAL | 7.5 mg in 1 1 | 2/23/2016 | |
| UCB, Inc. | 0091-3715 | ORAL | 15 mg in 1 1 | 2/23/2016 | |
| Glenmark Pharmaceuticals Inc., USA | 68462-209 | ORAL | 7.5 mg in 1 1 | 8/18/2021 | |
| Glenmark Pharmaceuticals Inc., USA | 68462-208 | ORAL | 15 mg in 1 1 | 8/18/2021 | |
| Physicians Total Care, Inc. | 54868-4883 | ORAL | 15 mg in 1 1 | 4/14/2011 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||