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API SUPPLIERS
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
HRV Pharma - Market Expansion Leader in Pharmaceuticals.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
About the Company : Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product gro...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
About the Company : Founded in 1984, DRL is well-known for its generic APIs and its track record in drug product development. It is one of the earliest pharma API manufacturers with a diverse portfoli...
HRV Pharma - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Pharma is a global manufacturer, seller, and exporter of APIs, intermediates, pellets, food-grade chemicals, food additives, and food ingredients. The company provides sourcing...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Drugs in Development
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PharmaCompass offers a list of Iptacopan Hydrochloride 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 Iptacopan Hydrochloride manufacturer or Iptacopan Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iptacopan Hydrochloride manufacturer or Iptacopan Hydrochloride supplier.
PharmaCompass also assists you with knowing the Iptacopan Hydrochloride API Price utilized in the formulation of products. Iptacopan Hydrochloride API Price is not always fixed or binding as the Iptacopan Hydrochloride Price is obtained through a variety of data sources. The Iptacopan Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LNP023 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LNP023, including repackagers and relabelers. The FDA regulates LNP023 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LNP023 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 LNP023 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LNP023 supplier is an individual or a company that provides LNP023 active pharmaceutical ingredient (API) or LNP023 finished formulations upon request. The LNP023 suppliers may include LNP023 API manufacturers, exporters, distributors and traders.
click here to find a list of LNP023 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 LNP023 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for LNP023 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 LNP023 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 LNP023 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LNP023 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of LNP023 suppliers with NDC on PharmaCompass.
LNP023 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 LNP023 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 LNP023 GMP manufacturer or LNP023 GMP API supplier for your needs.
A LNP023 CoA (Certificate of Analysis) is a formal document that attests to LNP023's compliance with LNP023 specifications and serves as a tool for batch-level quality control.
LNP023 CoA mostly includes findings from lab analyses of a specific batch. For each LNP023 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.
LNP023 may be tested according to a variety of international standards, such as European Pharmacopoeia (LNP023 EP), LNP023 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (LNP023 USP).
