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01 1Bioseutica B.V.
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01 1Lysozyme HCl
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01 1Netherlands
NDC Package Code : 84319-103
Start Marketing Date : 2024-05-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Lysozyme Chloride 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 Lysozyme Chloride manufacturer or Lysozyme Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lysozyme Chloride manufacturer or Lysozyme Chloride supplier.
PharmaCompass also assists you with knowing the Lysozyme Chloride API Price utilized in the formulation of products. Lysozyme Chloride API Price is not always fixed or binding as the Lysozyme Chloride Price is obtained through a variety of data sources. The Lysozyme Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lysozyme HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lysozyme HCl, including repackagers and relabelers. The FDA regulates Lysozyme HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lysozyme HCl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Lysozyme HCl supplier is an individual or a company that provides Lysozyme HCl active pharmaceutical ingredient (API) or Lysozyme HCl finished formulations upon request. The Lysozyme HCl suppliers may include Lysozyme HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Lysozyme HCl 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 Lysozyme HCl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lysozyme HCl 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 Lysozyme HCl 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 Lysozyme HCl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lysozyme HCl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lysozyme HCl suppliers with NDC on PharmaCompass.
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