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PharmaCompass offers a list of Clemastine 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 Clemastine manufacturer or Clemastine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clemastine manufacturer or Clemastine supplier.
PharmaCompass also assists you with knowing the Clemastine API Price utilized in the formulation of products. Clemastine API Price is not always fixed or binding as the Clemastine Price is obtained through a variety of data sources. The Clemastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clemastine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clemastine, including repackagers and relabelers. The FDA regulates Clemastine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clemastine 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 Clemastine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clemastine supplier is an individual or a company that provides Clemastine active pharmaceutical ingredient (API) or Clemastine finished formulations upon request. The Clemastine suppliers may include Clemastine API manufacturers, exporters, distributors and traders.
click here to find a list of Clemastine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clemastine CEP of the European Pharmacopoeia monograph is often referred to as a Clemastine Certificate of Suitability (COS). The purpose of a Clemastine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clemastine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clemastine to their clients by showing that a Clemastine CEP has been issued for it. The manufacturer submits a Clemastine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clemastine CEP holder for the record. Additionally, the data presented in the Clemastine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clemastine DMF.
A Clemastine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clemastine 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 Clemastine suppliers with CEP (COS) on PharmaCompass.
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