LEBSA- Your strategic API source for niche molecules.
01 1Laboratorios Espinos Y Bofill S.A. Cornella de Llobregat ES
02 2LABORATORIUM OFICHEM B.V. Ter Apel NL
LEBSA- Your strategic API source for niche molecules.
Certificate Number : CEP 2016-054 - Rev 01
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 143
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Certificate Number : R0-CEP 2020-131 - Rev 00
Status : Valid
Issue Date : 2023-01-25
Type : Chemical
Substance Number : 143
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Histamine Dihydrochloride, Process 1857
Certificate Number : CEP 2024-122 - Rev 00
Status : Valid
Issue Date : 2024-07-02
Type : Chemical
Substance Number : 143
87
PharmaCompass offers a list of Histamine Dihydrochloride 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 Histamine Dihydrochloride manufacturer or Histamine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Histamine Dihydrochloride manufacturer or Histamine Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Histamine Dihydrochloride API Price utilized in the formulation of products. Histamine Dihydrochloride API Price is not always fixed or binding as the Histamine Dihydrochloride Price is obtained through a variety of data sources. The Histamine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Histamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine, including repackagers and relabelers. The FDA regulates Histamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine 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 Histamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine supplier is an individual or a company that provides Histamine active pharmaceutical ingredient (API) or Histamine finished formulations upon request. The Histamine suppliers may include Histamine API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Histamine CEP of the European Pharmacopoeia monograph is often referred to as a Histamine Certificate of Suitability (COS). The purpose of a Histamine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Histamine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Histamine to their clients by showing that a Histamine CEP has been issued for it. The manufacturer submits a Histamine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Histamine CEP holder for the record. Additionally, the data presented in the Histamine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Histamine DMF.
A Histamine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Histamine 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 Histamine suppliers with CEP (COS) on PharmaCompass.
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