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01 1OLON S.P.A. Rodano IT
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01 1Cyproheptadine hydrochloride 1.5-hydrate
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01 1Italy
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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
87
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 Peritol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Peritol, including repackagers and relabelers. The FDA regulates Peritol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Peritol 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 Peritol supplier is an individual or a company that provides Peritol active pharmaceutical ingredient (API) or Peritol finished formulations upon request. The Peritol suppliers may include Peritol API manufacturers, exporters, distributors and traders.
click here to find a list of Peritol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Peritol CEP of the European Pharmacopoeia monograph is often referred to as a Peritol Certificate of Suitability (COS). The purpose of a Peritol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Peritol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Peritol to their clients by showing that a Peritol CEP has been issued for it. The manufacturer submits a Peritol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Peritol CEP holder for the record. Additionally, the data presented in the Peritol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Peritol DMF.
A Peritol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Peritol 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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