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