Overview
A homolog of ergonovine containing one more CH2 group. (Merck Index, 11th ed)
Indication
For the prevention and control of excessive bleeding following vaginal childbirth
Associated Conditions
- Angina Pectoris, Variant
- Postpartum Haemorrhage (PPH)
- Postpartum uterine subinvolution
- Uterine Atony
- Uterine Hemorrhage
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/03/16 | Phase 4 | Completed | |||
2019/04/05 | Phase 4 | Completed | |||
2018/07/12 | Phase 4 | Active, not recruiting | |||
2017/10/05 | Early Phase 1 | Withdrawn | |||
2015/04/06 | Phase 4 | Completed | |||
2009/03/10 | Not Applicable | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Amneal Pharmaceuticals NY LLC | 69238-1605 | ORAL | 0.2 mg in 1 1 | 6/12/2025 | |
Dispensing Solutions, Inc. | 66336-402 | ORAL | 0.2 mg in 1 1 | 9/22/2011 | |
Rising Pharma Holdings, Inc. | 16571-735 | ORAL | 0.2 mg in 1 1 | 11/24/2021 | |
Apotheca, Inc. | 12634-179 | ORAL | 0.2 mg in 1 1 | 2/19/2010 | |
Breckenridge Pharmaceutical, Inc. | 51991-144 | INTRAVENOUS | 0.2 mg in 1 mL | 2/20/2024 | |
Granules Pharmaceuticals Inc. | 70010-786 | ORAL | 0.2 mg in 1 1 | 7/26/2023 | |
ATLANTIC BIOLOGICALS CORP. | 17856-3655 | ORAL | 0.2 mg in 1 1 | 1/31/2020 | |
Pharmacist Pharmaceutical, LLC | 63704-006 | ORAL | 0.2 mg in 1 1 | 5/26/2011 | |
Novel Laboratories, Inc. | 40032-140 | ORAL | 0.2 mg in 1 1 | 12/22/2017 | |
Teva Pharmaceuticals USA, Inc. | 0093-3655 | ORAL | 0.2 mg in 1 1 | 7/1/2018 |
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. |
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