MedPath

Flurandrenolide

Generic Name
Flurandrenolide
Brand Names
Cordran, Nolix
Drug Type
Small Molecule
Chemical Formula
C24H33FO6
CAS Number
1524-88-5
Unique Ingredient Identifier
8EUL29XUQT

Overview

A corticosteroid used topically in the treatment of various skin disorders. It is usually employed as a cream or an ointment, and is also used as a polyethylene tape with an adhesive. (From Martindale, The Extra Pharmacopoeia, 30th ed, p733)

Indication

For relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses, particularly dry, scaling localized lesions

Associated Conditions

  • Dermatosis

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
Teligent Pharma, Inc.
52565-017
TOPICAL
0.5 mg in 1 g
9/10/2019
Almirall, LLC
16110-052
TOPICAL
0.5 mg in 1 mL
7/5/2018
Almirall, LLC
16110-034
TOPICAL
0.25 mg in 1 g
1/13/2023
Bryant Ranch Prepack
72162-1439
TOPICAL
0.5 mg in 1 mL
8/17/2023
Almirall, LLC
16110-587
TOPICAL
4 ug in 1 cm2
9/27/2019
Almirall, LLC
16110-035
TOPICAL
0.5 mg in 1 g
1/13/2023
Padagis Israel Pharmaceuticals Ltd
45802-928
TOPICAL
0.5 mg in 1 mL
10/11/2022
Taro Pharmaceuticals U.S.A., Inc.
51672-5301
TOPICAL
0.5 mg in 1 g
4/28/2016
Allergan, Inc.
0023-5870
TOPICAL
4 ug in 1 cm2
12/13/2019
INA Pharmaceutics, Inc
74157-130
TOPICAL
0.5 mg in 1 g
7/7/2025

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
DRENISON TAPE M 170 4MCG SQ CM
eli lilly canada inc
00128724
Tape - Topical
4 MCG / SQ CM
12/31/1969

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.