MedPath

Meprobamate

Generic Name
Meprobamate
Brand Names
Equagesic
Drug Type
Small Molecule
Chemical Formula
C9H18N2O4
CAS Number
57-53-4
Unique Ingredient Identifier
9I7LNY769Q

Overview

A carbamate with hypnotic, sedative, and some muscle relaxant properties, although in therapeutic doses reduction of anxiety rather than a direct effect may be responsible for muscle relaxation. Meprobamate has been reported to have anticonvulsant actions against petit mal seizures, but not against grand mal seizures (which may be exacerbated). It is used in the treatment of anxiety disorders, and also for the short-term management of insomnia but has largely been superseded by the benzodiazepines. (From Martindale, The Extra Pharmacopoeia, 30th ed, p603) Meprobamate is a controlled substance in the U.S.

Indication

For the management of anxiety disorders or for the short-term relief of the symptoms of anxiety.

Associated Conditions

  • Anxiety Disorders
  • Pain

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Taro Pharmaceuticals U.S.A., Inc.
51672-4147
ORAL
200 mg in 1 1
1/15/2019
Cipla USA Inc.
69097-974
ORAL
200 mg in 1 1
6/19/2021
Dr.Reddy's Laboratories Limited
55111-640
ORAL
200 mg in 1 1
9/9/2009
Dr.Reddy's Laboratories Limited
55111-641
ORAL
400 mg in 1 1
9/9/2009
Taro Pharmaceuticals U.S.A., Inc.
51672-4148
ORAL
400 mg in 1 1
1/15/2019
Alembic Pharmaceuticals Inc.
62332-020
ORAL
400 mg in 1 1
10/1/2021
Taro Pharmaceutical Industries Ltd.
52549-4147
ORAL
200 mg in 1 1
7/19/2011
Cipla USA Inc.
69097-975
ORAL
400 mg in 1 1
6/19/2021
Alembic Pharmaceuticals Inc.
62332-019
ORAL
200 mg in 1 1
10/1/2021
Alembic Pharmaceuticals Limited
46708-019
ORAL
200 mg in 1 1
1/10/2023

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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
APO MEPROBAMATE TAB 400MG
00337943
Tablet - Oral
400 MG / TAB
12/31/1975
NOVO-MEPRO 400MG
novopharm limited
00021547
Tablet - Oral
400 MG
12/31/1967
MEPROBAMATE TAB 400MG
PRO DOC LIMITEE
00156620
Tablet - Oral
400 MG / TAB
12/31/1959
MEPROBAMATE TAB 400MG
00431095
Tablet - Oral
400 MG / TAB
12/31/1978
282 MEP TAB
merck frosst canada & cie, merck frosst canada & co.
00108316
Tablet - Oral
200 MG
12/31/1959
NOVO-MEPRO 200MG
novopharm limited
00021539
Tablet - Oral
200 MG
12/31/1967
MEDITRAN 400MG
medic laboratory ltée
00134368
Tablet - Oral
400 MG
12/31/1959
EQUAGESIC TABLETS
wyeth-ayerst canada inc.
02041804
Tablet - Oral
200 MG / TAB
12/31/1995
EQUANIL TABLETS 400MG
wyeth-ayerst canada inc.
02041812
Tablet - Oral
400 MG / TAB
12/31/1994

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

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.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.