Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratorium Ofichem BV
01 1Palmitoylethanolamide
01 1Netherlands
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-1309
Start Marketing Date : 2018-07-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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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.
A Palmitamide MEA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Palmitamide MEA, including repackagers and relabelers. The FDA regulates Palmitamide MEA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Palmitamide MEA 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 Palmitamide MEA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Palmitamide MEA supplier is an individual or a company that provides Palmitamide MEA active pharmaceutical ingredient (API) or Palmitamide MEA finished formulations upon request. The Palmitamide MEA suppliers may include Palmitamide MEA API manufacturers, exporters, distributors and traders.
click here to find a list of Palmitamide MEA 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 Palmitamide MEA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Palmitamide MEA 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 Palmitamide MEA 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 Palmitamide MEA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Palmitamide MEA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Palmitamide MEA suppliers with NDC on PharmaCompass.
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