01 1OLON S.P.A. Rodano IT
01 1Cyproheptadine hydrochloride 1.5-hydrate
01 1Italy
01 1Valid
Cyproheptadine Hydrochloride 1.5-hydrate
Certificate Number : R1-CEP 2014-049 - Rev 01
Status : Valid
Issue Date : 2022-01-25
Type : Chemical
Substance Number : 817
A Cyproheptadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyproheptadine Hydrochloride, including repackagers and relabelers. The FDA regulates Cyproheptadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyproheptadine Hydrochloride 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 Cyproheptadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyproheptadine Hydrochloride supplier is an individual or a company that provides Cyproheptadine Hydrochloride active pharmaceutical ingredient (API) or Cyproheptadine Hydrochloride finished formulations upon request. The Cyproheptadine Hydrochloride suppliers may include Cyproheptadine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cyproheptadine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cyproheptadine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Cyproheptadine Hydrochloride Certificate of Suitability (COS). The purpose of a Cyproheptadine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cyproheptadine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cyproheptadine Hydrochloride to their clients by showing that a Cyproheptadine Hydrochloride CEP has been issued for it. The manufacturer submits a Cyproheptadine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cyproheptadine Hydrochloride CEP holder for the record. Additionally, the data presented in the Cyproheptadine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cyproheptadine Hydrochloride DMF.
A Cyproheptadine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cyproheptadine Hydrochloride 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 Cyproheptadine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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