01 1CHEMISCH-PHARMAZEUTISCHES LABOR, ROLF SACHSE GMBH Berlin DE
02 1FINORTEX, S.L. Sant Llorenç d’Hortons ES
03 1Interquim S.A. DE C.V. Estado De Mexico MX
01 3Detomidine hydrochloride for veterinary use
01 1Mexico
02 2Spain
01 3Valid
Detomidine Hydrochloride For Veterinary Use
Certificate Number : R0-CEP 2019-225 - Rev 00
Status : Valid
Issue Date : 2021-07-07
Type : Chemical
Substance Number : 1414
Detomidine Hydrochloride For Veterinary Use
Certificate Number : R0-CEP 2022-324 - Rev 00
Status : Valid
Issue Date : 2023-08-31
Type : Chemical
Substance Number : 1414
Detomidine Hydrochloride For Veterinary Use
Certificate Number : CEP 2022-044 - Rev 00
Status : Valid
Issue Date : 2023-10-04
Type : Chemical
Substance Number : 1414
A Detomidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Detomidine, including repackagers and relabelers. The FDA regulates Detomidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Detomidine 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 Detomidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Detomidine supplier is an individual or a company that provides Detomidine active pharmaceutical ingredient (API) or Detomidine finished formulations upon request. The Detomidine suppliers may include Detomidine API manufacturers, exporters, distributors and traders.
click here to find a list of Detomidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Detomidine CEP of the European Pharmacopoeia monograph is often referred to as a Detomidine Certificate of Suitability (COS). The purpose of a Detomidine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Detomidine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Detomidine to their clients by showing that a Detomidine CEP has been issued for it. The manufacturer submits a Detomidine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Detomidine CEP holder for the record. Additionally, the data presented in the Detomidine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Detomidine DMF.
A Detomidine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Detomidine 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 Detomidine suppliers with CEP (COS) on PharmaCompass.
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