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