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 1Azelis Deutschland Pharma GmbH Krefeld DE
03 2ERCROS S.A. Aranjuez ES
04 1JOYANG LABORATORIES Yancheng CN
05 3LEO PHARMA A/S Ballerup DK
01 2Fusidic acid
02 1Fusidic acid, Micronised
03 1Fusidic acid, Micronised, Process II
04 1Fusidic acid, Micronised, sterile
05 1Fusidic acid, Non-micronised and micronised
06 1Fusidic acid, Powder, Micronised
07 1Fusidic acid, Process B
08 1Fusidic acid, Sterile Powder and Sterile Micronized
01 3China
02 3Denmark
03 2Spain
04 1United Kingdom
01 7Valid
02 2Withdrawn 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 2022-330 - Rev 01
Status : Valid
Issue Date : 2024-10-15
Type : Chemical
Substance Number : 798
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.
Fusidic Acid, Non-micronised And Micronised
Certificate Number : R0-CEP 2019-139 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2021-10-27
Type : Chemical
Substance Number : 798
Certificate Number : R1-CEP 2003-182 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2012-03-16
Type : Chemical
Substance Number : 798
Fusidic Acid, Powder, Micronised
Certificate Number : R1-CEP 2006-121 - Rev 02
Status : Valid
Issue Date : 2021-11-17
Type : Chemical
Substance Number : 798
Fusidic Acid, Sterile Powder And Sterile Microni...
Certificate Number : CEP 2023-222 - Rev 00
Status : Valid
Issue Date : 2023-09-28
Type : Chemical
Substance Number : 798
Certificate Number : CEP 2014-046 - Rev 01
Status : Valid
Issue Date : 2024-04-22
Type : Chemical
Substance Number : 798
Fusidic Acid, Micronised, Sterile
Certificate Number : R1-CEP 2009-379 - Rev 00
Status : Valid
Issue Date : 2016-10-21
Type : Chemical
Substance Number : 798
Fusidic Acid, Micronised, Process II
Certificate Number : R0-CEP 2021-040 - Rev 01
Status : Valid
Issue Date : 2022-01-19
Type : Chemical
Substance Number : 798
Certificate Number : R1-CEP 2009-308 - Rev 02
Status : Valid
Issue Date : 2022-01-19
Type : Chemical
Substance Number : 798
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PharmaCompass offers a list of Fusidic Acid 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 Fusidic Acid manufacturer or Fusidic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Fusidic Acid API Price utilized in the formulation of products. Fusidic Acid API Price is not always fixed or binding as the Fusidic Acid Price is obtained through a variety of data sources. The Fusidic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diethanolamine fusidate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diethanolamine fusidate, including repackagers and relabelers. The FDA regulates Diethanolamine fusidate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diethanolamine 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 Diethanolamine fusidate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diethanolamine fusidate supplier is an individual or a company that provides Diethanolamine fusidate active pharmaceutical ingredient (API) or Diethanolamine fusidate finished formulations upon request. The Diethanolamine fusidate suppliers may include Diethanolamine fusidate API manufacturers, exporters, distributors and traders.
click here to find a list of Diethanolamine fusidate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diethanolamine fusidate CEP of the European Pharmacopoeia monograph is often referred to as a Diethanolamine fusidate Certificate of Suitability (COS). The purpose of a Diethanolamine fusidate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Diethanolamine fusidate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Diethanolamine fusidate to their clients by showing that a Diethanolamine fusidate CEP has been issued for it. The manufacturer submits a Diethanolamine fusidate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Diethanolamine fusidate CEP holder for the record. Additionally, the data presented in the Diethanolamine fusidate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Diethanolamine fusidate DMF.
A Diethanolamine fusidate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Diethanolamine 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 Diethanolamine fusidate suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering Diethanolamine fusidate
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