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