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