Close
4

Athena Athena

X

Find Mometasone Furoate manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
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

API REF. PRICE (USD / KG)
INTERMEDIATES
DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

Europe

Europe

Canada

Canada

Australia

Australia

South Africa

South Africa

Uploaded Dossiers

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

Annual Reports

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

USFDA Exclusivities

DIGITAL CONTENT

Blog #PharmaFlow

0

News

REF STANDARD

EDQM

USP

JP

0

Other Listed Suppliers

SERVICES

0

left grey arrow
right gray arrow
  • OINTMENT;TOPICAL - 0.1%
  • CREAM;TOPICAL - 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • LOTION;TOPICAL - 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • AEROSOL, METERED;INHALATION - 0.05MG/INH
  • AEROSOL, METERED;INHALATION - 0.10MG/INH
  • AEROSOL, METERED;INHALATION - 0.20MG/INH
  • SPRAY, METERED;NASAL - 0.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • POWDER;INHALATION - 0.11MG/INH
  • POWDER;INHALATION - 0.22MG/INH
  • AEROSOL, METERED;INHALATION - 0.005MG/INH;0.05MG/INH
  • AEROSOL, METERED;INHALATION - 0.005MG/INH;0.1MG/INH
  • AEROSOL, METERED;INHALATION - 0.005MG/INH;0.2MG/INH

Looking for 83919-23-7 / Mometasone Furoate API manufacturers, exporters & distributors?

Mometasone Furoate manufacturers, exporters & distributors 1

91

PharmaCompass offers a list of Mometasone Furoate 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 Mometasone Furoate manufacturer or Mometasone Furoate supplier for your needs.

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

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

API | Excipient name

Mometasone Furoate

Synonyms

83919-23-7, Asmanex, Nasonex, Elocon, Monovo, Sch 32088

Cas Number

83919-23-7

Unique Ingredient Identifier (UNII)

04201GDN4R

About Mometasone Furoate

A pregnadienediol derivative ANTI-ALLERGIC AGENT and ANTI-INFLAMMATORY AGENT that is used in the management of ASTHMA and ALLERGIC RHINITIS. It is also used as a topical treatment for skin disorders.

04201GDN4R Manufacturers

A 04201GDN4R manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04201GDN4R, including repackagers and relabelers. The FDA regulates 04201GDN4R manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04201GDN4R 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 04201GDN4R manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

04201GDN4R Suppliers

A 04201GDN4R supplier is an individual or a company that provides 04201GDN4R active pharmaceutical ingredient (API) or 04201GDN4R finished formulations upon request. The 04201GDN4R suppliers may include 04201GDN4R API manufacturers, exporters, distributors and traders.

click here to find a list of 04201GDN4R suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

04201GDN4R USDMF

A 04201GDN4R DMF (Drug Master File) is a document detailing the whole manufacturing process of 04201GDN4R active pharmaceutical ingredient (API) in detail. Different forms of 04201GDN4R DMFs exist exist since differing nations have different regulations, such as 04201GDN4R USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 04201GDN4R DMF submitted to regulatory agencies in the US is known as a USDMF. 04201GDN4R USDMF includes data on 04201GDN4R's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 04201GDN4R USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 04201GDN4R suppliers with USDMF on PharmaCompass.

04201GDN4R JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The 04201GDN4R Drug Master File in Japan (04201GDN4R JDMF) empowers 04201GDN4R API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the 04201GDN4R JDMF during the approval evaluation for pharmaceutical products. At the time of 04201GDN4R JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of 04201GDN4R suppliers with JDMF on PharmaCompass.

04201GDN4R KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a 04201GDN4R Drug Master File in Korea (04201GDN4R KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 04201GDN4R. The MFDS reviews the 04201GDN4R KDMF as part of the drug registration process and uses the information provided in the 04201GDN4R KDMF to evaluate the safety and efficacy of the drug.

After submitting a 04201GDN4R KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their 04201GDN4R API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 04201GDN4R suppliers with KDMF on PharmaCompass.

04201GDN4R CEP

A 04201GDN4R CEP of the European Pharmacopoeia monograph is often referred to as a 04201GDN4R Certificate of Suitability (COS). The purpose of a 04201GDN4R CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 04201GDN4R EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 04201GDN4R to their clients by showing that a 04201GDN4R CEP has been issued for it. The manufacturer submits a 04201GDN4R CEP (COS) as part of the market authorization procedure, and it takes on the role of a 04201GDN4R CEP holder for the record. Additionally, the data presented in the 04201GDN4R CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 04201GDN4R DMF.

A 04201GDN4R CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 04201GDN4R CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of 04201GDN4R suppliers with CEP (COS) on PharmaCompass.

04201GDN4R WC

A 04201GDN4R written confirmation (04201GDN4R WC) is an official document issued by a regulatory agency to a 04201GDN4R manufacturer, verifying that the manufacturing facility of a 04201GDN4R active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 04201GDN4R APIs or 04201GDN4R finished pharmaceutical products to another nation, regulatory agencies frequently require a 04201GDN4R WC (written confirmation) as part of the regulatory process.

click here to find a list of 04201GDN4R suppliers with Written Confirmation (WC) on PharmaCompass.

04201GDN4R 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 04201GDN4R as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 04201GDN4R 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 04201GDN4R 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 04201GDN4R and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 04201GDN4R NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 04201GDN4R suppliers with NDC on PharmaCompass.

04201GDN4R GMP

04201GDN4R 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 04201GDN4R 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 04201GDN4R GMP manufacturer or 04201GDN4R GMP API supplier for your needs.

04201GDN4R CoA

A 04201GDN4R CoA (Certificate of Analysis) is a formal document that attests to 04201GDN4R's compliance with 04201GDN4R specifications and serves as a tool for batch-level quality control.

04201GDN4R CoA mostly includes findings from lab analyses of a specific batch. For each 04201GDN4R 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.

04201GDN4R may be tested according to a variety of international standards, such as European Pharmacopoeia (04201GDN4R EP), 04201GDN4R JP (Japanese Pharmacopeia) and the US Pharmacopoeia (04201GDN4R 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
POST ENQUIRY