MedPath

Methyldopa

Generic Name
Methyldopa
Drug Type
Small Molecule
Chemical Formula
C10H13NO4
CAS Number
555-30-6
Unique Ingredient Identifier
M4R0H12F6M

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Withdrawn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Withdrawn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Withdrawn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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