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