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PharmaCompass offers a list of NONOXYNOL-9 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 NONOXYNOL-9 manufacturer or NONOXYNOL-9 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred NONOXYNOL-9 manufacturer or NONOXYNOL-9 supplier.
PharmaCompass also assists you with knowing the NONOXYNOL-9 API Price utilized in the formulation of products. NONOXYNOL-9 API Price is not always fixed or binding as the NONOXYNOL-9 Price is obtained through a variety of data sources. The NONOXYNOL-9 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nonoxynol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nonoxynol, including repackagers and relabelers. The FDA regulates Nonoxynol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nonoxynol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Nonoxynol supplier is an individual or a company that provides Nonoxynol active pharmaceutical ingredient (API) or Nonoxynol finished formulations upon request. The Nonoxynol suppliers may include Nonoxynol API manufacturers, exporters, distributors and traders.
click here to find a list of Nonoxynol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nonoxynol DMF (Drug Master File) is a document detailing the whole manufacturing process of Nonoxynol active pharmaceutical ingredient (API) in detail. Different forms of Nonoxynol DMFs exist exist since differing nations have different regulations, such as Nonoxynol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nonoxynol DMF submitted to regulatory agencies in the US is known as a USDMF. Nonoxynol USDMF includes data on Nonoxynol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nonoxynol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nonoxynol suppliers with USDMF on PharmaCompass.
A Nonoxynol CEP of the European Pharmacopoeia monograph is often referred to as a Nonoxynol Certificate of Suitability (COS). The purpose of a Nonoxynol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nonoxynol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nonoxynol to their clients by showing that a Nonoxynol CEP has been issued for it. The manufacturer submits a Nonoxynol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nonoxynol CEP holder for the record. Additionally, the data presented in the Nonoxynol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nonoxynol DMF.
A Nonoxynol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nonoxynol 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 Nonoxynol suppliers with CEP (COS) on PharmaCompass.
Nonoxynol 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 Nonoxynol 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 Nonoxynol GMP manufacturer or Nonoxynol GMP API supplier for your needs.
A Nonoxynol CoA (Certificate of Analysis) is a formal document that attests to Nonoxynol's compliance with Nonoxynol specifications and serves as a tool for batch-level quality control.
Nonoxynol CoA mostly includes findings from lab analyses of a specific batch. For each Nonoxynol 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.
Nonoxynol may be tested according to a variety of international standards, such as European Pharmacopoeia (Nonoxynol EP), Nonoxynol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nonoxynol USP).
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