MedPath

Hydrocortisone valerate

Generic Name
Hydrocortisone valerate
Brand Names
Hydroval
Drug Type
Small Molecule
Chemical Formula
C26H38O6
CAS Number
57524-89-7
Unique Ingredient Identifier
68717P8FUZ

Overview

No overview information available.

Indication

For the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Also used to treat endocrine (hormonal) disorders (adrenal insufficiency, Addisons disease). It is also used to treat many immune and allergic disorders, such as arthritis, lupus, severe psoriasis, severe asthma, ulcerative colitis, and Crohn's disease.

Associated Conditions

  • 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
Rebel Distributors Corp
21695-730
TOPICAL
2 mg in 1 g
9/25/2008
Cosette Pharmaceuticals, Inc.
0713-0560
TOPICAL
2 mg in 1 g
11/29/2023
A-S Medication Solutions
50090-2525
TOPICAL
2 mg in 1 g
1/10/2017
Physicians Total Care, Inc.
54868-5251
TOPICAL
2 mg in 1 g
10/29/2010
Physicians Total Care, Inc.
54868-4451
TOPICAL
2 mg in 1 g
10/29/2010
DIRECT RX
61919-010
TOPICAL
2 mg in 1 g
1/20/2020
Taro Pharmaceuticals U.S.A., Inc.
51672-1292
TOPICAL
2 mg in 1 g
1/25/2023
Encube Ethicals Private Limited
21922-007
TOPICAL
2 mg in 1 g
12/28/2022
Lupin Pharmaceuticals, Inc.
68180-954
TOPICAL
2 mg in 1 g
12/5/2019
Cosette Pharmaceuticals, Inc.
0713-0720
TOPICAL
2 mg in 1 g
11/29/2023

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
HYDROVAL OINTMENT 0.2%
taropharma, a division of taro pharmaceuticals inc.
02242985
Ointment - Topical
0.2 %
12/18/2000
WESTCORT ONT 0.2%
westwood-squibb, division of bristol-myers squibb canada inc.
01910132
Ointment - Topical
0.2 %
12/31/1991
WESTCORT CRM 0.2%
westwood-squibb, division of bristol-myers squibb canada inc.
01910124
Cream - Topical
0.2 %
12/31/1992
HYDROVAL CREAM 0.2%
taropharma, a division of taro pharmaceuticals inc.
02242984
Cream - Topical
0.2 %
12/18/2000

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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