01 1ZENJI PHARMACEUTICALS SUZHOU LTD. Suzhou CN
01 1Pentoxyverine hydrogen citrate
01 1Blank
01 1Valid
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Pentoxyverine Hydrogen Citrate
Certificate Number : CEP 2024-099 - Rev 01
Status : Valid
Issue Date : 2025-12-09
Type : Chemical
Substance Number : 1621
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PharmaCompass offers a list of Pentoxiverine citrate 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 Pentoxiverine citrate manufacturer or Pentoxiverine citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentoxiverine citrate manufacturer or Pentoxiverine citrate supplier.
PharmaCompass also assists you with knowing the Pentoxiverine citrate API Price utilized in the formulation of products. Pentoxiverine citrate API Price is not always fixed or binding as the Pentoxiverine citrate Price is obtained through a variety of data sources. The Pentoxiverine citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pentoxiverine citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentoxiverine citrate, including repackagers and relabelers. The FDA regulates Pentoxiverine citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentoxiverine citrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Pentoxiverine citrate supplier is an individual or a company that provides Pentoxiverine citrate active pharmaceutical ingredient (API) or Pentoxiverine citrate finished formulations upon request. The Pentoxiverine citrate suppliers may include Pentoxiverine citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Pentoxiverine citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pentoxiverine citrate CEP of the European Pharmacopoeia monograph is often referred to as a Pentoxiverine citrate Certificate of Suitability (COS). The purpose of a Pentoxiverine citrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Pentoxiverine citrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Pentoxiverine citrate to their clients by showing that a Pentoxiverine citrate CEP has been issued for it. The manufacturer submits a Pentoxiverine citrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Pentoxiverine citrate CEP holder for the record. Additionally, the data presented in the Pentoxiverine citrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Pentoxiverine citrate DMF.
A Pentoxiverine citrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Pentoxiverine citrate 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 Pentoxiverine citrate suppliers with CEP (COS) on PharmaCompass.
