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Status : Withdrawn by Holder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Status : Withdrawn by Holder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 : R0-CEP 2021-042 - Rev 00
Status : Valid
Issue Date : 2021-06-04
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 2009-380 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-11-14
Type : Chemical
Substance Number : 848
A Sodium Fusidate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Fusidate, including repackagers and relabelers. The FDA regulates Sodium Fusidate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Fusidate 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 Sodium Fusidate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Fusidate supplier is an individual or a company that provides Sodium Fusidate active pharmaceutical ingredient (API) or Sodium Fusidate finished formulations upon request. The Sodium Fusidate suppliers may include Sodium Fusidate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Fusidate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Fusidate CEP of the European Pharmacopoeia monograph is often referred to as a Sodium Fusidate Certificate of Suitability (COS). The purpose of a Sodium Fusidate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sodium Fusidate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sodium Fusidate to their clients by showing that a Sodium Fusidate CEP has been issued for it. The manufacturer submits a Sodium Fusidate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sodium Fusidate CEP holder for the record. Additionally, the data presented in the Sodium Fusidate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sodium Fusidate DMF.
A Sodium Fusidate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sodium Fusidate 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 Sodium Fusidate suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering Sodium Fusidate
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