01 1IMCD SWITZERLAND AG Zürich CH
02 1NANTONG HAIERS PHARMACEUTICAL CO., LTD. Nantong CN
03 1NANTONG JINGHUA PHARMACEUTICAL CO., LTD. Nantong CN
04 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 3Fluorouracil
02 1Fluorouracil, Micronised, non-micronised
01 2China
02 1Israel
03 1Netherlands
01 3Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Fluorouracil, Micronised, Non-micronised
Certificate Number : R1-CEP 2000-092 - Rev 07
Status : Valid
Issue Date : 2021-07-16
Type : Chemical
Substance Number : 611
Certificate Number : R1-CEP 2008-183 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2014-10-31
Type : Chemical
Substance Number : 611
Certificate Number : R1-CEP 2000-033 - Rev 07
Status : Valid
Issue Date : 2022-05-13
Type : Chemical
Substance Number : 611
Certificate Number : R1-CEP 2005-113 - Rev 05
Status : Valid
Issue Date : 2021-11-22
Type : Chemical
Substance Number : 611
22
PharmaCompass offers a list of Fluorouracil 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 Fluorouracil manufacturer or Fluorouracil supplier for your needs.
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PharmaCompass also assists you with knowing the Fluorouracil API Price utilized in the formulation of products. Fluorouracil API Price is not always fixed or binding as the Fluorouracil Price is obtained through a variety of data sources. The Fluorouracil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CAS-51-21-8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-51-21-8, including repackagers and relabelers. The FDA regulates CAS-51-21-8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-51-21-8 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 CAS-51-21-8 supplier is an individual or a company that provides CAS-51-21-8 active pharmaceutical ingredient (API) or CAS-51-21-8 finished formulations upon request. The CAS-51-21-8 suppliers may include CAS-51-21-8 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-51-21-8 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CAS-51-21-8 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-51-21-8 Certificate of Suitability (COS). The purpose of a CAS-51-21-8 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-51-21-8 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-51-21-8 to their clients by showing that a CAS-51-21-8 CEP has been issued for it. The manufacturer submits a CAS-51-21-8 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-51-21-8 CEP holder for the record. Additionally, the data presented in the CAS-51-21-8 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-51-21-8 DMF.
A CAS-51-21-8 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-51-21-8 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 CAS-51-21-8 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering CAS-51-21-8
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