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PharmaCompass offers a list of Isotretinoin 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 Isotretinoin manufacturer or Isotretinoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isotretinoin manufacturer or Isotretinoin supplier.
PharmaCompass also assists you with knowing the Isotretinoin API Price utilized in the formulation of products. Isotretinoin API Price is not always fixed or binding as the Isotretinoin Price is obtained through a variety of data sources. The Isotretinoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Claravis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Claravis, including repackagers and relabelers. The FDA regulates Claravis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Claravis 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 Claravis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Claravis supplier is an individual or a company that provides Claravis active pharmaceutical ingredient (API) or Claravis finished formulations upon request. The Claravis suppliers may include Claravis API manufacturers, exporters, distributors and traders.
click here to find a list of Claravis suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Claravis CEP of the European Pharmacopoeia monograph is often referred to as a Claravis Certificate of Suitability (COS). The purpose of a Claravis CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Claravis EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Claravis to their clients by showing that a Claravis CEP has been issued for it. The manufacturer submits a Claravis CEP (COS) as part of the market authorization procedure, and it takes on the role of a Claravis CEP holder for the record. Additionally, the data presented in the Claravis CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Claravis DMF.
A Claravis CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Claravis 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 Claravis suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Claravis
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