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Looking for 544-31-0 / Palmitoylethanolamide API manufacturers, exporters & distributors?

Palmitoylethanolamide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Palmitoylethanolamide 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 Palmitoylethanolamide manufacturer or Palmitoylethanolamide supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Palmitoylethanolamide manufacturer or Palmitoylethanolamide supplier.

PharmaCompass also assists you with knowing the Palmitoylethanolamide API Price utilized in the formulation of products. Palmitoylethanolamide API Price is not always fixed or binding as the Palmitoylethanolamide Price is obtained through a variety of data sources. The Palmitoylethanolamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Palmitoylethanolamide

Synonyms

Palmidrol, 544-31-0, N-(2-hydroxyethyl)hexadecanamide, Palmitoyl ethanolamide, Impulsin, Palmitamide mea

Cas Number

544-31-0

Unique Ingredient Identifier (UNII)

6R8T1UDM3V

About Palmitoylethanolamide

Palmitoyl ethanolamide is a metabolite found in the aging mouse brain.

Palmitoyl ethanolamide Manufacturers

A Palmitoyl ethanolamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Palmitoyl ethanolamide, including repackagers and relabelers. The FDA regulates Palmitoyl ethanolamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Palmitoyl ethanolamide 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 Palmitoyl ethanolamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Palmitoyl ethanolamide Suppliers

A Palmitoyl ethanolamide supplier is an individual or a company that provides Palmitoyl ethanolamide active pharmaceutical ingredient (API) or Palmitoyl ethanolamide finished formulations upon request. The Palmitoyl ethanolamide suppliers may include Palmitoyl ethanolamide API manufacturers, exporters, distributors and traders.

click here to find a list of Palmitoyl ethanolamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Palmitoyl ethanolamide NDC

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 Palmitoyl ethanolamide as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Palmitoyl ethanolamide API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Palmitoyl ethanolamide 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Palmitoyl ethanolamide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Palmitoyl ethanolamide NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Palmitoyl ethanolamide suppliers with NDC on PharmaCompass.

Palmitoyl ethanolamide GMP

Palmitoyl ethanolamide 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 Palmitoyl ethanolamide 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 Palmitoyl ethanolamide GMP manufacturer or Palmitoyl ethanolamide GMP API supplier for your needs.

Palmitoyl ethanolamide CoA

A Palmitoyl ethanolamide CoA (Certificate of Analysis) is a formal document that attests to Palmitoyl ethanolamide's compliance with Palmitoyl ethanolamide specifications and serves as a tool for batch-level quality control.

Palmitoyl ethanolamide CoA mostly includes findings from lab analyses of a specific batch. For each Palmitoyl ethanolamide 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.

Palmitoyl ethanolamide may be tested according to a variety of international standards, such as European Pharmacopoeia (Palmitoyl ethanolamide EP), Palmitoyl ethanolamide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Palmitoyl ethanolamide USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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