Quotient Sciences Quotient Sciences


Find Desonide manufacturers, exporters & distributors on PharmaCompass

API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications


JDMFs Filed

JDMFs Filed


Other Certificates

Other Certificates

Other Suppliers

Other Suppliers



USA (Orange Book)

USA (Orange Book)








South Africa

South Africa

Uploaded Dossiers

Uploaded Dossiers


U.S. Medicaid

Annual Reports



USFDA Orange Book Patents

USFDA Exclusivities



Blog #PharmaFlow









Other Listed Suppliers



left grey arrow
right gray arrow
  • CREAM;TOPICAL - 0.05%
  • GEL;TOPICAL - 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 638-94-8 / Desonide API manufacturers, exporters & distributors?

Desonide manufacturers, exporters & distributors 1


PharmaCompass offers a list of Desonide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Desonide manufacturer or Desonide supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desonide manufacturer or Desonide supplier.

PharmaCompass also assists you with knowing the Desonide API Price utilized in the formulation of products. Desonide API Price is not always fixed or binding as the Desonide Price is obtained through a variety of data sources. The Desonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name



638-94-8, Prednacinolone, Locapred, Desowen, Desonate, Topifug

Cas Number


Unique Ingredient Identifier (UNII)


About Desonide

A nonfluorinated corticosteroid anti-inflammatory agent used topically for DERMATOSES.

Desonide Manufacturers

A Desonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desonide, including repackagers and relabelers. The FDA regulates Desonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desonide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Desonide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Desonide Suppliers

A Desonide supplier is an individual or a company that provides Desonide active pharmaceutical ingredient (API) or Desonide finished formulations upon request. The Desonide suppliers may include Desonide API manufacturers, exporters, distributors and traders.

click here to find a list of Desonide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Desonide USDMF

A Desonide DMF (Drug Master File) is a document detailing the whole manufacturing process of Desonide active pharmaceutical ingredient (API) in detail. Different forms of Desonide DMFs exist exist since differing nations have different regulations, such as Desonide USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Desonide DMF submitted to regulatory agencies in the US is known as a USDMF. Desonide USDMF includes data on Desonide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Desonide USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Desonide suppliers with USDMF on PharmaCompass.

Desonide WC

A Desonide written confirmation (Desonide WC) is an official document issued by a regulatory agency to a Desonide manufacturer, verifying that the manufacturing facility of a Desonide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Desonide APIs or Desonide finished pharmaceutical products to another nation, regulatory agencies frequently require a Desonide WC (written confirmation) as part of the regulatory process.

click here to find a list of Desonide suppliers with Written Confirmation (WC) on PharmaCompass.

Desonide NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Desonide as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Desonide API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Desonide as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Desonide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Desonide NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Desonide suppliers with NDC on PharmaCompass.

Desonide GMP

Desonide Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Desonide GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Desonide GMP manufacturer or Desonide GMP API supplier for your needs.

Desonide CoA

A Desonide CoA (Certificate of Analysis) is a formal document that attests to Desonide's compliance with Desonide specifications and serves as a tool for batch-level quality control.

Desonide CoA mostly includes findings from lab analyses of a specific batch. For each Desonide CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Desonide may be tested according to a variety of international standards, such as European Pharmacopoeia (Desonide EP), Desonide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Desonide USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry