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