Aspen API. More than just an API.
01 1ASPEN OSS B.V. Oss NL
02 1BACHEM AMERICAS, INC. Torrance US
03 1AURO PEPTIDES LIMITED Kandi Mandal IN
04 1BCN PEPTIDES S.A. St Quinti De Mediona ES
05 1HYBIO PHARMACEUTICAL CO., LTD. Shenzhen CN
06 2Lonza Braine S.A. Braine-L'Alleud BE
07 1MYLAN LABORATORIES LIMITED Hyderabad IN
08 1Mallinckrodt Inc St Louis US
09 1PIRAMAL PHARMA LIMITED Mumbai IN
10 1POLYPEPTIDE S.A. Braine-L'Alleud BE
11 2PolyPeptide Laboratories (Sweden) AB Limhamn SE
12 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
13 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 10Desmopressin
02 1Desmopressin, 40001
03 1Desmopressin, 41006
04 1Desmopressin, Liquid phase synthesis process
05 1Desmopressin, Liquid phase synthesis process , Process F
06 1Desmopressin, Solid phase synthesis process
01 1Belgium
02 1China
03 4India
04 1Israel
05 1Netherlands
06 1Spain
07 2Sweden
08 3Switzerland
09 1U.S.A
01 1Expired
02 11Valid
03 3Withdrawn by Holder
Certificate Number : R1-CEP 1999-165 - Rev 05
Status : Valid
Issue Date : 2016-03-31
Type : Chemical
Substance Number : 712
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Certificate Number : R1-CEP 2007-157 - Rev 02
Status : Valid
Issue Date : 2023-06-29
Type : Chemical
Substance Number : 712
Certificate Number : R1-CEP 2016-125 - Rev 01
Status : Valid
Issue Date : 2023-03-31
Type : Chemical
Substance Number : 712
Certificate Number : R1-CEP 2002-058 - Rev 02
Status : Valid
Issue Date : 2008-09-02
Type : Chemical
Substance Number : 712
Certificate Number : R0-CEP 2021-221 - Rev 00
Status : Valid
Issue Date : 2022-11-14
Type : Chemical
Substance Number : 712
Desmopressin, Liquid Phase Synthesis Process
Certificate Number : R1-CEP 2003-208 - Rev 01
Status : Valid
Issue Date : 2011-03-04
Type : Chemical
Substance Number : 712
Certificate Number : R1-CEP 2009-087 - Rev 02
Status : Valid
Issue Date : 2022-10-04
Type : Chemical
Substance Number : 712
Certificate Number : R1-CEP 2006-266 - Rev 00
Status : Valid
Issue Date : 2013-11-27
Type : Chemical and TSE
Substance Number : 712
Certificate Number : CEP 2024-028 - Rev 00
Status : Valid
Issue Date : 2024-10-03
Type : Chemical
Substance Number : 712
Certificate Number : R1-CEP 2006-113 - Rev 03
Status : Valid
Issue Date : 2021-10-07
Type : Chemical
Substance Number : 712
A Desmopressin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desmopressin Acetate, including repackagers and relabelers. The FDA regulates Desmopressin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desmopressin Acetate 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 Desmopressin Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desmopressin Acetate supplier is an individual or a company that provides Desmopressin Acetate active pharmaceutical ingredient (API) or Desmopressin Acetate finished formulations upon request. The Desmopressin Acetate suppliers may include Desmopressin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Desmopressin Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Desmopressin Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Desmopressin Acetate Certificate of Suitability (COS). The purpose of a Desmopressin Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Desmopressin Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Desmopressin Acetate to their clients by showing that a Desmopressin Acetate CEP has been issued for it. The manufacturer submits a Desmopressin Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Desmopressin Acetate CEP holder for the record. Additionally, the data presented in the Desmopressin Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Desmopressin Acetate DMF.
A Desmopressin Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Desmopressin Acetate 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 Desmopressin Acetate suppliers with CEP (COS) on PharmaCompass.
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