01 1F.I.S. - Fabbrica Italiana Sintetici S.p.A. Montecchio Maggiore IT
01 1Prazepam
01 1Italy
01 1Valid
Certificate Number : CEP 2023-291 - Rev 00
Status : Valid
Issue Date : 2025-06-20
Type : Chemical
Substance Number : 1466
95
PharmaCompass offers a list of Prazepam 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 Prazepam manufacturer or Prazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prazepam manufacturer or Prazepam supplier.
PharmaCompass also assists you with knowing the Prazepam API Price utilized in the formulation of products. Prazepam API Price is not always fixed or binding as the Prazepam Price is obtained through a variety of data sources. The Prazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lysanxia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lysanxia, including repackagers and relabelers. The FDA regulates Lysanxia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lysanxia 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 Lysanxia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lysanxia supplier is an individual or a company that provides Lysanxia active pharmaceutical ingredient (API) or Lysanxia finished formulations upon request. The Lysanxia suppliers may include Lysanxia API manufacturers, exporters, distributors and traders.
click here to find a list of Lysanxia suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lysanxia CEP of the European Pharmacopoeia monograph is often referred to as a Lysanxia Certificate of Suitability (COS). The purpose of a Lysanxia CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lysanxia EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lysanxia to their clients by showing that a Lysanxia CEP has been issued for it. The manufacturer submits a Lysanxia CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lysanxia CEP holder for the record. Additionally, the data presented in the Lysanxia CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lysanxia DMF.
A Lysanxia CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lysanxia CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Lysanxia suppliers with CEP (COS) on PharmaCompass.
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