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