01 ASPEN OSS B.V. Oss NL (1)
02 BACHEM AMERICAS, INC. Torrance US (1)
03 PIRAMAL PHARMA LIMITED Mumbai IN (1)
04 AURO PEPTIDES LIMITED Kandi Mandal IN (1)
05 BCN PEPTIDES S.A. St Quinti De Mediona ES (1)
06 HYBIO PHARMACEUTICAL CO., LTD. Shenzhen CN (1)
07 Lonza Braine S.A. Braine-L'Alleud BE (2)
08 MYLAN LABORATORIES LIMITED Hyderabad IN (1)
09 Mallinckrodt Inc St Louis US (1)
10 POLYPEPTIDE S.A. Braine-L'Alleud BE (1)
11 PolyPeptide Laboratories (Sweden) AB Limhamn SE (2)
12 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (1)
01 Desmopressin (9)
02 Desmopressin, 40001 (1)
03 Desmopressin, 41006 (1)
04 Desmopressin, Liquid phase synthesis process (1)
05 Desmopressin, Liquid phase synthesis process , Process F (1)
06 Desmopressin, Solid phase synthesis process (1)
01 Belgium (1)
02 China (1)
03 India (3)
04 Israel (1)
05 Netherlands (1)
06 Spain (1)
07 Sweden (2)
08 Switzerland (3)
09 U.S.A (1)
01 Expired (1)
02 Valid (10)
03 Withdrawn by Holder (3)
37
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 CONCENTRAID manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CONCENTRAID, including repackagers and relabelers. The FDA regulates CONCENTRAID manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CONCENTRAID 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 CONCENTRAID manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CONCENTRAID supplier is an individual or a company that provides CONCENTRAID active pharmaceutical ingredient (API) or CONCENTRAID finished formulations upon request. The CONCENTRAID suppliers may include CONCENTRAID API manufacturers, exporters, distributors and traders.
click here to find a list of CONCENTRAID suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CONCENTRAID CEP of the European Pharmacopoeia monograph is often referred to as a CONCENTRAID Certificate of Suitability (COS). The purpose of a CONCENTRAID CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CONCENTRAID EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CONCENTRAID to their clients by showing that a CONCENTRAID CEP has been issued for it. The manufacturer submits a CONCENTRAID CEP (COS) as part of the market authorization procedure, and it takes on the role of a CONCENTRAID CEP holder for the record. Additionally, the data presented in the CONCENTRAID CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CONCENTRAID DMF.
A CONCENTRAID CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CONCENTRAID CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 11 companies offering CONCENTRAID
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