01 1Fagron Inc
02 1Professional Compounding Centers of America
03 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
01 2Pyridoxal-5-Phosphate
02 1Pyridoxal-5-Phosphate Mono
01 1Italy
02 1Netherlands
03 1United Kingdom
NDC Package Code : 51552-1404
Start Marketing Date : 2011-10-31
End Marketing Date : 2025-06-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-5184
Start Marketing Date : 2022-04-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12711-7490
Start Marketing Date : 1993-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of Pyridoxal Phosphate 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 Pyridoxal Phosphate manufacturer or Pyridoxal Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pyridoxal Phosphate manufacturer or Pyridoxal Phosphate supplier.
PharmaCompass also assists you with knowing the Pyridoxal Phosphate API Price utilized in the formulation of products. Pyridoxal Phosphate API Price is not always fixed or binding as the Pyridoxal Phosphate Price is obtained through a variety of data sources. The Pyridoxal Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PLP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PLP, including repackagers and relabelers. The FDA regulates PLP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PLP 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 PLP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PLP supplier is an individual or a company that provides PLP active pharmaceutical ingredient (API) or PLP finished formulations upon request. The PLP suppliers may include PLP API manufacturers, exporters, distributors and traders.
click here to find a list of PLP 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 PLP as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PLP 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 PLP 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 PLP and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PLP NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PLP suppliers with NDC on PharmaCompass.
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