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