MedPath

Metaxalone

Generic Name
Metaxalone
Brand Names
Skelaxin
Drug Type
Small Molecule
Chemical Formula
C12H15NO3
CAS Number
1665-48-1
Unique Ingredient Identifier
1NMA9J598Y

Overview

Metaxalone is a moderate to strong muscle relaxant used in the symptomatic treatment of musculoskeletal pain caused by strains, sprains, and other musculoskeletal conditions. It is marketed by King Pharmaceuticals under the brand name Skelaxin®. Its main mechanism of action is thought to involve general central nervous system depression. Metaxalone is associated with few side effects and is available as a 800 mg scored tablet.

Background

Metaxalone is a moderate to strong muscle relaxant used in the symptomatic treatment of musculoskeletal pain caused by strains, sprains, and other musculoskeletal conditions. It is marketed by King Pharmaceuticals under the brand name Skelaxin®. Its main mechanism of action is thought to involve general central nervous system depression. Metaxalone is associated with few side effects and is available as a 800 mg scored tablet.

Indication

临床主要用作炎症、外伤等引起的局部肌肉痉挛性疼痛的辅助用药。

Associated Conditions

  • Pain

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
California Pharmaceuticals, LLC
70332-330
ORAL
800 mg in 1 1
1/2/2018
Advanced Rx Pharmacy of Tennessee, LLC
80425-0131
ORAL
800 mg in 1 1
11/10/2022
Bryant Ranch Prepack
63629-8014
ORAL
800 mg in 1 1
5/12/2020
American Health Packaging
60687-663
ORAL
800 mg in 1 1
3/3/2023
Northwind Pharmaceuticals
51655-162
ORAL
800 mg in 1 1
6/17/2014
Amneal Pharmaceuticals of New York LLC
53746-553
ORAL
800 mg in 1 1
1/11/2023
Quality Care Products, LLC
55700-911
ORAL
800 mg in 1 1
11/18/2022
RedPharm Drug, Inc.
67296-0993
ORAL
800 mg in 1 1
1/20/2022
Advanced Rx Pharmacy of Tennessee, LLC
80425-0122
ORAL
800 mg in 1 1
2/8/2023
Physicians Total Care, Inc.
54868-6102
ORAL
800 mg in 1 1
5/17/2011

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
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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