Overview
Methyldopa, or α-methyldopa, is a centrally acting sympatholytic agent and an antihypertensive agent. It is an analog of DOPA (3,4‐hydroxyphenylanine), and it is a prodrug, meaning that the drug requires biotransformation to an active metabolite for therapeutic effects. Methyldopa works by binding to alpha(α)-2 adrenergic receptors as an agonist, leading to the inhibition of adrenergic neuronal outflow and reduction of vasoconstrictor adrenergic signals. Methyldopa exists in two isomers D-α-methyldopa and L-α-methyldopa, which is the active form. First introduced in 1960 as an antihypertensive agent, methyldopa was considered to be useful in certain patient populations, such as pregnant women and patients with renal insufficiency. Since then, methyldopa was largely replaced by newer, better-tolerated antihypertensive agents; however, it is still used as monotherapy or in combination with hydrochlorothiazide. Methyldopa is also available as intravenous injection, which is used to manage hypertension when oral therapy is unfeasible and to treat hypertensive crisis.
Indication
Methyldopa is indicated for the management of hypertension as monotherapy or in combination with hydrochlorothiazide. Methyldopa injection is used to manage hypertensive crises.
Associated Conditions
- Hypertension
- Hypertensive crisis
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2021/04/08 | Phase 4 | Completed | Federal University of Paraíba | ||
2018/01/11 | Phase 2 | Withdrawn | |||
2015/08/24 | Phase 4 | UNKNOWN | |||
2013/07/31 | Phase 4 | Completed | Gynuity Health Projects | ||
2013/07/30 | Not Applicable | Completed | |||
2013/06/21 | Not Applicable | Completed | |||
2012/08/28 | Phase 2 | Completed | |||
2007/12/27 | Phase 1 | Completed | |||
2006/05/24 | Not Applicable | Withdrawn | Afshan B. Hameed, M.D. | ||
2005/09/19 | Phase 1 | Withdrawn |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Chartwell RX, LLC | 62135-322 | ORAL | 500 mg in 1 1 | 1/4/2023 | |
Rebel Distributors Corp | 42254-351 | ORAL | 250 mg in 1 1 | 8/3/2007 | |
Physicians Total Care, Inc. | 54868-1328 | ORAL | 500 mg in 1 1 | 3/22/2011 | |
Chartwell RX, LLC | 62135-321 | ORAL | 250 mg in 1 1 | 1/4/2023 | |
Rebel Distributors Corp | 21695-880 | ORAL | 500 mg in 1 1 | 8/3/2007 | |
Carilion Materials Management | 68151-2791 | ORAL | 250 mg in 1 1 | 12/3/2015 | |
Rebel Distributors Corp | 21695-879 | ORAL | 250 mg in 1 1 | 8/3/2007 | |
Physicians Total Care, Inc. | 54868-0050 | ORAL | 250 mg in 1 1 | 3/22/2011 |
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 |
---|---|---|---|---|---|
AA PHARMA METHYLDOPA TABLET 250 mg | SIN03618P | TABLET, FILM COATED | 250 mg | 7/15/1989 |
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. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
MEDIMET 250TAB | medic laboratory ltée | 00385077 | Tablet - Oral | 250 MG | 12/31/1976 |
PMS-DOPAZIDE-25 TAB | 00584975 | Tablet - Oral | 250 MG | 12/31/1984 | |
ALDOMET TAB 500MG | merck frosst canada & cie, merck frosst canada & co. | 00016586 | Tablet - Oral | 500 MG | 12/31/1971 |
METHYLDOPA | aa pharma inc | 00360252 | Tablet - Oral | 125 MG | 4/2/1980 |
SUPRES 250 TAB | merck frosst canada & cie, merck frosst canada & co. | 00231177 | Tablet - Oral | 250 MG | 12/31/1972 |
METHYLDOPA TABLETS 125MG | 02232648 | Tablet - Oral | 125 MG | N/A | |
NU-MEDOPA TAB 125MG | nu-pharm inc | 00717517 | Tablet - Oral | 125 MG | 12/31/1990 |
PMS-DOPAZIDE 15 TAB | 00584967 | Tablet - Oral | 250 MG | 12/31/1984 | |
METHYLDOPA 125 TAB 125MG | PRO DOC LIMITEE | 00456365 | Tablet - Oral | 125 MG | 12/31/1978 |
SUPRES 150 TAB | merck frosst canada & cie, merck frosst canada & co. | 00231169 | Tablet - Oral | 250 MG | 12/31/1972 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
ALDOMET FORTE 500 MG COMPRIMIDOS RECUBIERTOS CON PELÍCULA | H.A.C. Pharma | 53587 | COMPRIMIDO RECUBIERTO | Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración | Commercialized |
ALDOMET 250 MG COMPRIMIDOS RECUBIERTOS CON PELÍCULA | H.A.C. Pharma | 37932 | COMPRIMIDO RECUBIERTO | Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración | Commercialized |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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