Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Aventis Pharma Deutschland GmbH Frankfurt Am Main DE
02 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
03 1VANI PHARMA LABS LIMITED Hyderabad IN
01 3Propyphenazone
01 1China
02 1France
03 1India
01 1Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R1-CEP 1998-088 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2004-12-07
Type : Chemical
Substance Number : 636
Certificate Number : R1-CEP 2003-059 - Rev 05
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 636
Certificate Number : R1-CEP 2001-041 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-01-23
Type : Chemical
Substance Number : 636
26
PharmaCompass offers a list of Propyphenazone 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 Propyphenazone manufacturer or Propyphenazone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propyphenazone manufacturer or Propyphenazone supplier.
PharmaCompass also assists you with knowing the Propyphenazone API Price utilized in the formulation of products. Propyphenazone API Price is not always fixed or binding as the Propyphenazone Price is obtained through a variety of data sources. The Propyphenazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Budirol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Budirol, including repackagers and relabelers. The FDA regulates Budirol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Budirol 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 Budirol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Budirol supplier is an individual or a company that provides Budirol active pharmaceutical ingredient (API) or Budirol finished formulations upon request. The Budirol suppliers may include Budirol API manufacturers, exporters, distributors and traders.
click here to find a list of Budirol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Budirol CEP of the European Pharmacopoeia monograph is often referred to as a Budirol Certificate of Suitability (COS). The purpose of a Budirol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Budirol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Budirol to their clients by showing that a Budirol CEP has been issued for it. The manufacturer submits a Budirol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Budirol CEP holder for the record. Additionally, the data presented in the Budirol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Budirol DMF.
A Budirol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Budirol 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 Budirol suppliers with CEP (COS) on PharmaCompass.
We have 3 companies offering Budirol
Get in contact with the supplier of your choice:
