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