Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
01 2FUJIAN COMHONY BIOTECHNOLOGY CO., LTD. Fuqing CN
02 1ERCROS S.A. Aranjuez ES
03 1JOYANG LABORATORIES Yancheng CN
04 5LEO PHARMA A/S Ballerup DK
05 1OJSC "Biosintez" Penza RU
01 3Sodium fusidate
02 1Sodium fusidate, Micronised
03 1Sodium fusidate, Micronised, Process II
04 1Sodium fusidate, Non-micronised and micronised
05 1Sodium fusidate, Powder, Micronised
06 1Sodium fusidate, Process B
07 1Sodium fusidate, Process II
08 1Sodium fusidate, Sterile
01 3China
02 5Denmark
03 1Russia
04 1Spain
01 7Valid
02 3Withdrawn by Holder
Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
Certificate Number : CEP 2022-369 - Rev 01
Status : Valid
Issue Date : 2024-11-04
Type : Chemical
Substance Number : 848
Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
Sodium Fusidate, Non-micronised And Micronised
Certificate Number : R0-CEP 2019-284 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2021-10-27
Type : Chemical
Substance Number : 848
Certificate Number : R1-CEP 2008-207 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2015-05-07
Type : Chemical
Substance Number : 848
Sodium Fusidate, Powder, Micronised
Certificate Number : R1-CEP 2006-120 - Rev 02
Status : Valid
Issue Date : 2022-02-18
Type : Chemical
Substance Number : 848
Certificate Number : CEP 2021-307 - Rev 01
Status : Valid
Issue Date : 2024-07-11
Type : Chemical
Substance Number : 848
Certificate Number : R1-CEP 2009-309 - Rev 00
Status : Valid
Issue Date : 2016-07-29
Type : Chemical
Substance Number : 848
Sodium Fusidate, Micronised, Process II
Certificate Number : R0-CEP 2021-041 - Rev 01
Status : Valid
Issue Date : 2022-01-19
Type : Chemical
Substance Number : 848
Certificate Number : R1-CEP 2009-317 - Rev 02
Status : Valid
Issue Date : 2022-01-19
Type : Chemical
Substance Number : 848
Certificate Number : R0-CEP 2021-042 - Rev 00
Status : Valid
Issue Date : 2021-06-04
Type : Chemical
Substance Number : 848
Certificate Number : R0-CEP 2009-380 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-11-14
Type : Chemical
Substance Number : 848
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PharmaCompass offers a list of Sodium Fusidate 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 Sodium Fusidate manufacturer or Sodium Fusidate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Fusidate API Price utilized in the formulation of products. Sodium Fusidate API Price is not always fixed or binding as the Sodium Fusidate Price is obtained through a variety of data sources. The Sodium Fusidate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fusin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fusin, including repackagers and relabelers. The FDA regulates Fusin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fusin 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 Fusin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fusin supplier is an individual or a company that provides Fusin active pharmaceutical ingredient (API) or Fusin finished formulations upon request. The Fusin suppliers may include Fusin API manufacturers, exporters, distributors and traders.
click here to find a list of Fusin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fusin CEP of the European Pharmacopoeia monograph is often referred to as a Fusin Certificate of Suitability (COS). The purpose of a Fusin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fusin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fusin to their clients by showing that a Fusin CEP has been issued for it. The manufacturer submits a Fusin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fusin CEP holder for the record. Additionally, the data presented in the Fusin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fusin DMF.
A Fusin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fusin 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 Fusin suppliers with CEP (COS) on PharmaCompass.
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