01 1CLAROCHEM IRELAND LTD. Dublin 15 IE
02 1F.I.S. - Fabbrica Italiana Sintetici S.p.A. Montecchio Maggiore IT
03 1Interquim S.A. DE C.V. Estado De Mexico MX
04 2LABIANA PHARMACEUTICALS, S.L.U. Corbera de Llobregat ES
05 1ZACH SYSTEM Avrillé FR
01 5Fosfomycin trometamol
02 1Fosfomycin trometamol, FT23
01 1France
02 1Ireland
03 1Italy
04 1Mexico
05 2Spain
01 6Valid
Certificate Number : R0-CEP 2022-327 - Rev 00
Status : Valid
Issue Date : 2023-05-17
Type : Chemical
Substance Number : 1425
Certificate Number : CEP 2015-289 - Rev 01
Status : Valid
Issue Date : 2024-10-30
Type : Chemical
Substance Number : 1425
Certificate Number : CEP 2017-166 - Rev 03
Status : Valid
Issue Date : 2024-08-02
Type : Chemical
Substance Number : 1425
Certificate Number : CEP 2012-265 - Rev 05
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 1425
Certificate Number : CEP 2023-068 - Rev 01
Status : Valid
Issue Date : 2024-03-04
Type : Chemical
Substance Number : 1425
Certificate Number : CEP 2020-370 - Rev 03
Status : Valid
Issue Date : 2024-06-12
Type : Chemical
Substance Number : 1425
14
PharmaCompass offers a list of Fosfomycin 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 Fosfomycin manufacturer or Fosfomycin supplier for your needs.
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A Monuril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monuril, including repackagers and relabelers. The FDA regulates Monuril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monuril 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 Monuril supplier is an individual or a company that provides Monuril active pharmaceutical ingredient (API) or Monuril finished formulations upon request. The Monuril suppliers may include Monuril API manufacturers, exporters, distributors and traders.
click here to find a list of Monuril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Monuril CEP of the European Pharmacopoeia monograph is often referred to as a Monuril Certificate of Suitability (COS). The purpose of a Monuril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Monuril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Monuril to their clients by showing that a Monuril CEP has been issued for it. The manufacturer submits a Monuril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Monuril CEP holder for the record. Additionally, the data presented in the Monuril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Monuril DMF.
A Monuril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Monuril 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 Monuril suppliers with CEP (COS) on PharmaCompass.
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