MedPath

Halcinonide

Generic Name
Halcinonide
Brand Names
Halog
Drug Type
Small Molecule
Chemical Formula
C24H32ClFO5
CAS Number
3093-35-4
Unique Ingredient Identifier
SI86V6QNEG

Overview

Halcinonide is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses, and is distributed as a cream and ointment. Halcinonide is marketed under the brand name Halog® by Ranbaxy Laboratories Inc. Research suggests that clobetasol propionate demonstrates superior pharmacologic efficacy in the treatment of psoriasis when compared to halcinonide.

Indication

Indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Associated Conditions

  • Dermatosis
  • Corticosteroid-responsive dermatoses

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
Sun Pharmaceutical Industries, Inc.
10631-094
TOPICAL
1 mg in 1 g
1/7/2019
Glasshouse Pharmaceuticals Limited Canada
71428-011
TOPICAL
1 mg in 1 g
1/9/2024
Sun Pharmaceutical Industries, Inc.
10631-096
TOPICAL
1 mg in 1 g
7/29/2019
Sun Pharmaceutical Industries, Inc.
10631-095
TOPICAL
1 mg in 1 mL
5/18/2021
Mylan Pharmaceuticals Inc.
0378-8056
TOPICAL
1 mg in 1 g
8/30/2019
Sun Pharmaceutical Industries, Inc.
57664-698
TOPICAL
1 mg in 1 g
5/27/2021

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
HALOG ONT 0.1%
bristol-myers squibb canada
02010283
Ointment - Topical
0.1 %
12/31/1977
HALOG CREAM 0.1%
bristol-myers squibb canada
02011921
Cream - Topical
0.1 %
12/31/1994
HALOG LIQ 0.1%
westwood-squibb, division of bristol-myers squibb canada inc.
02010291
Liquid - Topical
.1 %
12/31/1972

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.

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