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