Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
01 1FUJIAN COMHONY BIOTECHNOLOGY CO., LTD. Fuqing CN
02 1Azelis Deutschland Pharma GmbH Krefeld DE
03 1ERCROS 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, Powder, Micronised
06 1Fusidic acid, Process B
01 1China
02 3Denmark
03 1Spain
04 1United Kingdom
05 1Blank
01 6Valid
02 1Withdrawn 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 02
Status : Valid
Issue Date : 2025-09-22
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Status : Withdrawn by Holder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
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 : CEP 2021-040 - Rev 02
Status : Valid
Issue Date : 2026-05-12
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
97
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A Ramycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ramycin, including repackagers and relabelers. The FDA regulates Ramycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ramycin 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 Ramycin supplier is an individual or a company that provides Ramycin active pharmaceutical ingredient (API) or Ramycin finished formulations upon request. The Ramycin suppliers may include Ramycin API manufacturers, exporters, distributors and traders.
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A Ramycin CEP of the European Pharmacopoeia monograph is often referred to as a Ramycin Certificate of Suitability (COS). The purpose of a Ramycin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ramycin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ramycin to their clients by showing that a Ramycin CEP has been issued for it. The manufacturer submits a Ramycin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ramycin CEP holder for the record. Additionally, the data presented in the Ramycin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ramycin DMF.
A Ramycin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ramycin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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