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
01 2Histamine dihydrochloride
02 1Histamine dihydrochloride, Process 1857
01 2Netherlands
02 1Spain
01 3Valid
LEBSA- Your strategic API source for niche molecules.
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.
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.
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
A Histamine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine Dihydrochloride, including repackagers and relabelers. The FDA regulates Histamine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine Dihydrochloride 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 Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine Dihydrochloride supplier is an individual or a company that provides Histamine Dihydrochloride active pharmaceutical ingredient (API) or Histamine Dihydrochloride finished formulations upon request. The Histamine Dihydrochloride suppliers may include Histamine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Histamine Dihydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Histamine Dihydrochloride Certificate of Suitability (COS). The purpose of a Histamine Dihydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Histamine Dihydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Histamine Dihydrochloride to their clients by showing that a Histamine Dihydrochloride CEP has been issued for it. The manufacturer submits a Histamine Dihydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Histamine Dihydrochloride CEP holder for the record. Additionally, the data presented in the Histamine Dihydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Histamine Dihydrochloride DMF.
A Histamine Dihydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Histamine Dihydrochloride 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 Dihydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Histamine Dihydrochloride
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