01 1JANSSEN PHARMACEUTICA NV Beerse BE
02 1Joint Stock Company "Grindeks" Riga LV
01 2Droperidol
01 1Belgium
02 1Latvia
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2012-164 - Rev 02
Status : Valid
Issue Date : 2020-06-12
Type : Chemical
Substance Number : 1010
Certificate Number : R1-CEP 1997-062 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2006-11-15
Type : Chemical
Substance Number : 1010
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PharmaCompass offers a list of Droperidol 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 Droperidol manufacturer or Droperidol supplier for your needs.
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PharmaCompass also assists you with knowing the Droperidol API Price utilized in the formulation of products. Droperidol API Price is not always fixed or binding as the Droperidol Price is obtained through a variety of data sources. The Droperidol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FENTANYL CITRATE AND DROPERIDOL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FENTANYL CITRATE AND DROPERIDOL, including repackagers and relabelers. The FDA regulates FENTANYL CITRATE AND DROPERIDOL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FENTANYL CITRATE AND DROPERIDOL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A FENTANYL CITRATE AND DROPERIDOL supplier is an individual or a company that provides FENTANYL CITRATE AND DROPERIDOL active pharmaceutical ingredient (API) or FENTANYL CITRATE AND DROPERIDOL finished formulations upon request. The FENTANYL CITRATE AND DROPERIDOL suppliers may include FENTANYL CITRATE AND DROPERIDOL API manufacturers, exporters, distributors and traders.
click here to find a list of FENTANYL CITRATE AND DROPERIDOL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A FENTANYL CITRATE AND DROPERIDOL CEP of the European Pharmacopoeia monograph is often referred to as a FENTANYL CITRATE AND DROPERIDOL Certificate of Suitability (COS). The purpose of a FENTANYL CITRATE AND DROPERIDOL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of FENTANYL CITRATE AND DROPERIDOL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of FENTANYL CITRATE AND DROPERIDOL to their clients by showing that a FENTANYL CITRATE AND DROPERIDOL CEP has been issued for it. The manufacturer submits a FENTANYL CITRATE AND DROPERIDOL CEP (COS) as part of the market authorization procedure, and it takes on the role of a FENTANYL CITRATE AND DROPERIDOL CEP holder for the record. Additionally, the data presented in the FENTANYL CITRATE AND DROPERIDOL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the FENTANYL CITRATE AND DROPERIDOL DMF.
A FENTANYL CITRATE AND DROPERIDOL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. FENTANYL CITRATE AND DROPERIDOL 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 FENTANYL CITRATE AND DROPERIDOL suppliers with CEP (COS) on PharmaCompass.
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