Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 2Moehs Iberica S.L. Rubi ES
02 1Nycomed Austria GmbH Linz AT
01 3Celiprolol hydrochloride
01 1Austria
02 2Spain
01 1Valid
02 2Withdrawn by Holder
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 2007-220 - Rev 04
Status : Valid
Issue Date : 2024-03-08
Type : Chemical
Substance Number : 1632
Certificate Number : R0-CEP 2006-259 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2009-09-04
Type : Chemical
Substance Number : 1632
Certificate Number : R1-CEP 2004-294 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2013-10-11
Type : Chemical
Substance Number : 1632
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PharmaCompass offers a list of Celiprolol Hydrochloride 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 Celiprolol Hydrochloride manufacturer or Celiprolol Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Celiprolol Hydrochloride API Price utilized in the formulation of products. Celiprolol Hydrochloride API Price is not always fixed or binding as the Celiprolol Hydrochloride Price is obtained through a variety of data sources. The Celiprolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Selectrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selectrol, including repackagers and relabelers. The FDA regulates Selectrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selectrol 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 Selectrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selectrol supplier is an individual or a company that provides Selectrol active pharmaceutical ingredient (API) or Selectrol finished formulations upon request. The Selectrol suppliers may include Selectrol API manufacturers, exporters, distributors and traders.
click here to find a list of Selectrol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selectrol CEP of the European Pharmacopoeia monograph is often referred to as a Selectrol Certificate of Suitability (COS). The purpose of a Selectrol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Selectrol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Selectrol to their clients by showing that a Selectrol CEP has been issued for it. The manufacturer submits a Selectrol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Selectrol CEP holder for the record. Additionally, the data presented in the Selectrol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Selectrol DMF.
A Selectrol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Selectrol 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 Selectrol suppliers with CEP (COS) on PharmaCompass.
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