01 1OLON S.P.A. Rodano IT
01 1Cyproheptadine hydrochloride 1.5-hydrate
01 1Italy
01 1Valid
Cyproheptadine Hydrochloride 1.5-hydrate
Certificate Number : CEP 2014-049 - Rev 02
Status : Valid
Issue Date : 2025-02-05
Type : Chemical
Substance Number : 817
41
PharmaCompass offers a list of Cyproheptadine Hydrochloride 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 Cyproheptadine Hydrochloride manufacturer or Cyproheptadine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyproheptadine Hydrochloride manufacturer or Cyproheptadine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cyproheptadine Hydrochloride API Price utilized in the formulation of products. Cyproheptadine Hydrochloride API Price is not always fixed or binding as the Cyproheptadine Hydrochloride Price is obtained through a variety of data sources. The Cyproheptadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CYPROHEPTADINE HCL, manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CYPROHEPTADINE HCL,, including repackagers and relabelers. The FDA regulates CYPROHEPTADINE HCL, manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CYPROHEPTADINE HCL, 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 CYPROHEPTADINE HCL, supplier is an individual or a company that provides CYPROHEPTADINE HCL, active pharmaceutical ingredient (API) or CYPROHEPTADINE HCL, finished formulations upon request. The CYPROHEPTADINE HCL, suppliers may include CYPROHEPTADINE HCL, API manufacturers, exporters, distributors and traders.
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A CYPROHEPTADINE HCL, CEP of the European Pharmacopoeia monograph is often referred to as a CYPROHEPTADINE HCL, Certificate of Suitability (COS). The purpose of a CYPROHEPTADINE HCL, CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CYPROHEPTADINE HCL, EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CYPROHEPTADINE HCL, to their clients by showing that a CYPROHEPTADINE HCL, CEP has been issued for it. The manufacturer submits a CYPROHEPTADINE HCL, CEP (COS) as part of the market authorization procedure, and it takes on the role of a CYPROHEPTADINE HCL, CEP holder for the record. Additionally, the data presented in the CYPROHEPTADINE HCL, CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CYPROHEPTADINE HCL, DMF.
A CYPROHEPTADINE HCL, CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CYPROHEPTADINE HCL, CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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