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PharmaCompass offers a list of Desmopressin Acetate 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 Desmopressin Acetate manufacturer or Desmopressin Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desmopressin Acetate manufacturer or Desmopressin Acetate supplier.
PharmaCompass also assists you with knowing the Desmopressin Acetate API Price utilized in the formulation of products. Desmopressin Acetate API Price is not always fixed or binding as the Desmopressin Acetate Price is obtained through a variety of data sources. The Desmopressin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DDAVP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DDAVP, including repackagers and relabelers. The FDA regulates DDAVP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DDAVP 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 DDAVP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DDAVP supplier is an individual or a company that provides DDAVP active pharmaceutical ingredient (API) or DDAVP finished formulations upon request. The DDAVP suppliers may include DDAVP API manufacturers, exporters, distributors and traders.
click here to find a list of DDAVP suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DDAVP CEP of the European Pharmacopoeia monograph is often referred to as a DDAVP Certificate of Suitability (COS). The purpose of a DDAVP CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DDAVP EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DDAVP to their clients by showing that a DDAVP CEP has been issued for it. The manufacturer submits a DDAVP CEP (COS) as part of the market authorization procedure, and it takes on the role of a DDAVP CEP holder for the record. Additionally, the data presented in the DDAVP CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DDAVP DMF.
A DDAVP CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DDAVP 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 DDAVP suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering DDAVP
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