Midodrine
- Generic Name
- Midodrine
- Brand Names
- Proamatine
- Drug Type
- Small Molecule
- Chemical Formula
- C12H18N2O4
- CAS Number
- 42794-76-3
- Unique Ingredient Identifier
- 6YE7PBM15H
Overview
An ethanolamine derivative that is an adrenergic alpha agonist. It is used as a vasoconstrictor agent in the treatment of hypotension.
Background
An ethanolamine derivative that is an adrenergic alpha agonist. It is used as a vasoconstrictor agent in the treatment of hypotension.
Indication
For the treatment of symptomatic orthostatic hypotension (OH).
Associated Conditions
- Symptomatic Orthostatic Hypotension
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2018/10/15 | Phase 3 | Terminated | |||
2018/08/24 | Not Applicable | Completed | |||
2018/07/26 | Phase 1 | Completed | |||
2018/03/29 | Phase 1 | Recruiting | |||
2018/02/13 | Not Applicable | Completed | |||
2017/11/22 | Phase 4 | Completed | |||
2017/05/09 | Not Applicable | Completed | |||
2017/04/26 | Phase 1 | Completed | |||
2017/03/15 | Phase 4 | UNKNOWN | Nimedical | ||
2016/12/13 | Phase 3 | Withdrawn |
FDA Approved Products
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Product Name | Manufacturer | Route | Strength | Approved | NDC Code |
|---|---|---|---|---|---|
Drug Ocean LLC | ORAL | 2.5 mg in 1 1 | 2023/12/23 | 70985-006 | |
Drug Ocean LLC | ORAL | 10 mg in 1 1 | 2023/12/23 | 70985-007 | |
ORAL | 10 mg in 1 1 | 2018/10/30 | 49884-874 | ||
ORAL | 2.5 mg in 1 1 | 2018/10/30 | 49884-814 | ||
ORAL | 2.5 mg in 1 1 | 2024/03/26 | 68382-737 | ||
ORAL | 5 mg in 1 1 | 2024/01/25 | 55154-5696 | ||
ORAL | 10 mg in 1 1 | 2024/03/26 | 68382-739 | ||
ORAL | 5 mg in 1 1 | 2024/03/26 | 68382-738 | ||
ORAL | 2.5 mg in 1 1 | 2020/10/15 | 70700-157 | ||
ORAL | 10 mg in 1 1 | 2023/10/20 | 82293-005 |
EMA Approved Products
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Medicine Name | EMA Number | Auth. Holder | Country | Drug Type | Status | Issued | Opinion | Revision |
|---|
No EMA products found
No EMA products found for this drug
HSA Approved Products
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Product Name | Manufacturer | Dosage Form | Strength | Approved | Approval No. |
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NMPA Approved Products
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Product Name | Approval No. | Manufacturer | Dosage Form | Trade Name | Strength | Type | Status | Date | Import |
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No NMPA products found for this drug
PPB Approved Products
Product Name | Registration Code | Company | Category | Sale Type | Reg. Date |
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No PPB products found
No PPB products found for this drug
TGA Approved Products
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Product Name | ARTG ID | Sponsor | Status | Reg. Date | Ingredient |
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