API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
Other Suppliers
0
USA (Orange Book)
Europe
Canada
0
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
100
PharmaCompass offers a list of Diclofenac 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 Diclofenac manufacturer or Diclofenac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diclofenac manufacturer or Diclofenac supplier.
PharmaCompass also assists you with knowing the Diclofenac API Price utilized in the formulation of products. Diclofenac API Price is not always fixed or binding as the Diclofenac Price is obtained through a variety of data sources. The Diclofenac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Voltaren manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Voltaren, including repackagers and relabelers. The FDA regulates Voltaren manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Voltaren 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 Voltaren manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Voltaren supplier is an individual or a company that provides Voltaren active pharmaceutical ingredient (API) or Voltaren finished formulations upon request. The Voltaren suppliers may include Voltaren API manufacturers, exporters, distributors and traders.
click here to find a list of Voltaren suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Voltaren DMF (Drug Master File) is a document detailing the whole manufacturing process of Voltaren active pharmaceutical ingredient (API) in detail. Different forms of Voltaren DMFs exist exist since differing nations have different regulations, such as Voltaren USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Voltaren DMF submitted to regulatory agencies in the US is known as a USDMF. Voltaren USDMF includes data on Voltaren's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Voltaren USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Voltaren suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Voltaren Drug Master File in Korea (Voltaren KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Voltaren. The MFDS reviews the Voltaren KDMF as part of the drug registration process and uses the information provided in the Voltaren KDMF to evaluate the safety and efficacy of the drug.
After submitting a Voltaren 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 Voltaren API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Voltaren suppliers with KDMF on PharmaCompass.
A Voltaren written confirmation (Voltaren WC) is an official document issued by a regulatory agency to a Voltaren manufacturer, verifying that the manufacturing facility of a Voltaren active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Voltaren APIs or Voltaren finished pharmaceutical products to another nation, regulatory agencies frequently require a Voltaren WC (written confirmation) as part of the regulatory process.
click here to find a list of Voltaren suppliers with Written Confirmation (WC) on PharmaCompass.
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 Voltaren as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Voltaren API and other APIs are published in this directory by the FDA.
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 Voltaren 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.
The NDC directory also contains data on finished compounded human drug products that contain Voltaren and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Voltaren NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Voltaren suppliers with NDC on PharmaCompass.
Voltaren 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 Voltaren 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 Voltaren GMP manufacturer or Voltaren GMP API supplier for your needs.
A Voltaren CoA (Certificate of Analysis) is a formal document that attests to Voltaren's compliance with Voltaren specifications and serves as a tool for batch-level quality control.
Voltaren CoA mostly includes findings from lab analyses of a specific batch. For each Voltaren 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.
Voltaren may be tested according to a variety of international standards, such as European Pharmacopoeia (Voltaren EP), Voltaren JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Voltaren USP).