TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI NL B.V. Amsterdam NL
02 1IMCD SWITZERLAND AG Zürich CH
03 1NANTONG HAIERS PHARMACEUTICAL CO., LTD. Nantong CN
04 1NANTONG JINGHUA PHARMACEUTICAL CO., LTD. Nantong CN
01 3Fluorouracil
02 1Fluorouracil, Micronised, non-micronised
01 2China
02 1Israel
03 1Netherlands
01 3Valid
02 1Withdrawn by EDQM Failure to CEP procedure
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2005-113 - Rev 06
Status : Valid
Issue Date : 2025-03-10
Type : Chemical
Substance Number : 611
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Status : Withdrawn by EDQM Failure to CEP pro...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
100
PharmaCompass offers a list of Fluorouracil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Fluorouracil manufacturer or Fluorouracil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluorouracil manufacturer or Fluorouracil supplier.
A Timazin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Timazin, including repackagers and relabelers. The FDA regulates Timazin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Timazin 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 Timazin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Timazin supplier is an individual or a company that provides Timazin active pharmaceutical ingredient (API) or Timazin finished formulations upon request. The Timazin suppliers may include Timazin API manufacturers, exporters, distributors and traders.
click here to find a list of Timazin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Timazin CEP of the European Pharmacopoeia monograph is often referred to as a Timazin Certificate of Suitability (COS). The purpose of a Timazin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Timazin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Timazin to their clients by showing that a Timazin CEP has been issued for it. The manufacturer submits a Timazin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Timazin CEP holder for the record. Additionally, the data presented in the Timazin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Timazin DMF.
A Timazin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Timazin 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 Timazin suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Timazin
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