Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI WINTHROP INDUSTRIE Gentilly FR
02 1DERIVADOS QUIMICOS S.A.U. Alcantarilla ES
03 1NOSCH LABS PRIVATE LIMITED Hyderabad IN
01 3Ciprofibrate
01 1France
02 1India
03 1Spain
01 3Valid
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 : CEP 2011-120 - Rev 05
Status : Valid
Issue Date : 2024-04-17
Type : Chemical
Substance Number : 2013
Certificate Number : CEP 2013-112 - Rev 03
Status : Valid
Issue Date : 2024-05-03
Type : Chemical
Substance Number : 2013
Certificate Number : R0-CEP 2021-263 - Rev 00
Status : Valid
Issue Date : 2023-06-12
Type : Chemical
Substance Number : 2013
39
PharmaCompass offers a list of Ciprofibrate 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 Ciprofibrate manufacturer or Ciprofibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ciprofibrate manufacturer or Ciprofibrate supplier.
PharmaCompass also assists you with knowing the Ciprofibrate API Price utilized in the formulation of products. Ciprofibrate API Price is not always fixed or binding as the Ciprofibrate Price is obtained through a variety of data sources. The Ciprofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oroxadin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oroxadin, including repackagers and relabelers. The FDA regulates Oroxadin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oroxadin 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 Oroxadin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oroxadin supplier is an individual or a company that provides Oroxadin active pharmaceutical ingredient (API) or Oroxadin finished formulations upon request. The Oroxadin suppliers may include Oroxadin API manufacturers, exporters, distributors and traders.
click here to find a list of Oroxadin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oroxadin CEP of the European Pharmacopoeia monograph is often referred to as a Oroxadin Certificate of Suitability (COS). The purpose of a Oroxadin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oroxadin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oroxadin to their clients by showing that a Oroxadin CEP has been issued for it. The manufacturer submits a Oroxadin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oroxadin CEP holder for the record. Additionally, the data presented in the Oroxadin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oroxadin DMF.
A Oroxadin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oroxadin 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 Oroxadin suppliers with CEP (COS) on PharmaCompass.
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