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API SUPPLIERS
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Mitoxantrone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mitoxantrone, including repackagers and relabelers. The FDA regulates Mitoxantrone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mitoxantrone 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 Mitoxantrone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mitoxantrone supplier is an individual or a company that provides Mitoxantrone active pharmaceutical ingredient (API) or Mitoxantrone finished formulations upon request. The Mitoxantrone suppliers may include Mitoxantrone API manufacturers, exporters, distributors and traders.
click here to find a list of Mitoxantrone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mitoxantrone DMF (Drug Master File) is a document detailing the whole manufacturing process of Mitoxantrone active pharmaceutical ingredient (API) in detail. Different forms of Mitoxantrone DMFs exist exist since differing nations have different regulations, such as Mitoxantrone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Mitoxantrone DMF submitted to regulatory agencies in the US is known as a USDMF. Mitoxantrone USDMF includes data on Mitoxantrone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Mitoxantrone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Mitoxantrone suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Mitoxantrone Drug Master File in Japan (Mitoxantrone JDMF) empowers Mitoxantrone API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Mitoxantrone JDMF during the approval evaluation for pharmaceutical products. At the time of Mitoxantrone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Mitoxantrone suppliers with JDMF on PharmaCompass.
A Mitoxantrone CEP of the European Pharmacopoeia monograph is often referred to as a Mitoxantrone Certificate of Suitability (COS). The purpose of a Mitoxantrone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mitoxantrone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mitoxantrone to their clients by showing that a Mitoxantrone CEP has been issued for it. The manufacturer submits a Mitoxantrone CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mitoxantrone CEP holder for the record. Additionally, the data presented in the Mitoxantrone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mitoxantrone DMF.
A Mitoxantrone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mitoxantrone 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 Mitoxantrone 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 Mitoxantrone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mitoxantrone 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 Mitoxantrone 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 Mitoxantrone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mitoxantrone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mitoxantrone suppliers with NDC on PharmaCompass.
Mitoxantrone 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 Mitoxantrone 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 Mitoxantrone GMP manufacturer or Mitoxantrone GMP API supplier for your needs.
A Mitoxantrone CoA (Certificate of Analysis) is a formal document that attests to Mitoxantrone's compliance with Mitoxantrone specifications and serves as a tool for batch-level quality control.
Mitoxantrone CoA mostly includes findings from lab analyses of a specific batch. For each Mitoxantrone 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.
Mitoxantrone may be tested according to a variety of international standards, such as European Pharmacopoeia (Mitoxantrone EP), Mitoxantrone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mitoxantrone USP).
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