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API SUPPLIERS
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NDC API
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Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
About the Company : Laboratorium Ofichem is a GMP-certified and FDA-approved API manufacturer with state-of-the-art development and production facilities in the Netherlands. We develop and manufacture...
ASolution Pharmaceuticals: Your Partner for cGMP Development & Manufacturing Services – Supplying APIs, FDFs, and Specialty Molecules.
About the Company : Since 2010, our dedication to our clientele has been unwavering in addressing pharmaceutical hurdles, regardless of scale. We prioritize integrity, responsiveness, and punctuality,...
Gangwal Healthcare is powered by innovation, driving health, wellness & healing.
About the Company : Gangwal Healthcare – a solutions provider for Complex, Innovative & Cutting-edge technological formulations!
The building of a "best-in-class" solution provider starts wit...
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ABOUT THIS PAGE
A Palmidrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Palmidrol, including repackagers and relabelers. The FDA regulates Palmidrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Palmidrol 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 Palmidrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Palmidrol supplier is an individual or a company that provides Palmidrol active pharmaceutical ingredient (API) or Palmidrol finished formulations upon request. The Palmidrol suppliers may include Palmidrol API manufacturers, exporters, distributors and traders.
click here to find a list of Palmidrol 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 Palmidrol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Palmidrol 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 Palmidrol 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 Palmidrol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Palmidrol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Palmidrol suppliers with NDC on PharmaCompass.
Palmidrol 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 Palmidrol 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 Palmidrol GMP manufacturer or Palmidrol GMP API supplier for your needs.
A Palmidrol CoA (Certificate of Analysis) is a formal document that attests to Palmidrol's compliance with Palmidrol specifications and serves as a tool for batch-level quality control.
Palmidrol CoA mostly includes findings from lab analyses of a specific batch. For each Palmidrol 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.
Palmidrol may be tested according to a variety of international standards, such as European Pharmacopoeia (Palmidrol EP), Palmidrol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Palmidrol USP).
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