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ABOUT THIS PAGE
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PharmaCompass offers a list of Acyclovir Sodium 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 Acyclovir Sodium manufacturer or Acyclovir Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acyclovir Sodium manufacturer or Acyclovir Sodium supplier.
PharmaCompass also assists you with knowing the Acyclovir Sodium API Price utilized in the formulation of products. Acyclovir Sodium API Price is not always fixed or binding as the Acyclovir Sodium Price is obtained through a variety of data sources. The Acyclovir Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Viclovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viclovir, including repackagers and relabelers. The FDA regulates Viclovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viclovir 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 Viclovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Viclovir supplier is an individual or a company that provides Viclovir active pharmaceutical ingredient (API) or Viclovir finished formulations upon request. The Viclovir suppliers may include Viclovir API manufacturers, exporters, distributors and traders.
click here to find a list of Viclovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Viclovir DMF (Drug Master File) is a document detailing the whole manufacturing process of Viclovir active pharmaceutical ingredient (API) in detail. Different forms of Viclovir DMFs exist exist since differing nations have different regulations, such as Viclovir USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Viclovir DMF submitted to regulatory agencies in the US is known as a USDMF. Viclovir USDMF includes data on Viclovir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Viclovir USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Viclovir suppliers with USDMF on PharmaCompass.
A Viclovir written confirmation (Viclovir WC) is an official document issued by a regulatory agency to a Viclovir manufacturer, verifying that the manufacturing facility of a Viclovir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Viclovir APIs or Viclovir finished pharmaceutical products to another nation, regulatory agencies frequently require a Viclovir WC (written confirmation) as part of the regulatory process.
click here to find a list of Viclovir 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 Viclovir as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Viclovir 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 Viclovir 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 Viclovir and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Viclovir NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Viclovir suppliers with NDC on PharmaCompass.
Viclovir 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 Viclovir 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 Viclovir GMP manufacturer or Viclovir GMP API supplier for your needs.
A Viclovir CoA (Certificate of Analysis) is a formal document that attests to Viclovir's compliance with Viclovir specifications and serves as a tool for batch-level quality control.
Viclovir CoA mostly includes findings from lab analyses of a specific batch. For each Viclovir 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.
Viclovir may be tested according to a variety of international standards, such as European Pharmacopoeia (Viclovir EP), Viclovir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Viclovir USP).
