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