Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Reset all filters
01 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
02 1SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
03 2EUROAPI FRANCE Vertolaye FR
04 1BAYER AG Leverkusen DE
05 1CURIA SPAIN S.A.U. Boecillo ES
06 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
07 1Pharmacia & Upjohn Company Kalamazoo US
08 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
09 2TIANJIN JINJIN PHARMACEUTICAL CO., LTD. Zhangjiawo Town CN
10 1ZHEJIANG PURE PHARMACEUTICAL CO., LTD. Xianju CN
11 1ZHEJIANG XIANJU PHARMACEUTICAL CO., LTD. Xianju CN
Reset all filters
01 5Hydrocortisone
02 1Hydrocortisone, Micro 20
03 2Hydrocortisone, Micronised
04 1Hydrocortisone, Micronised, non-micronised
05 1Hydrocortisone, Micronised, process 2
06 2Hydrocortisone, Non-micronised, micronised
07 1Hydrocortisone, Process B, micronised, non-micronised
Reset all filters
01 6China
02 2France
03 1Germany
04 1India
05 3U.S.A
Reset all filters
01 12Valid
02 1Withdrawn by Holder
Hydrocortisone, Non-micronised, Micronised
Certificate Number : R1-CEP 2002-220 - Rev 02
Status : Valid
Issue Date : 2023-03-23
Type : Chemical
Substance Number : 335
Certificate Number : CEP 2018-054 - Rev 02
Status : Valid
Issue Date : 2024-04-15
Type : Chemical
Substance Number : 335
Hydrocortisone, Micronised, Process 2
Certificate Number : R1-CEP 2012-163 - Rev 01
Status : Valid
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 335
Certificate Number : CEP 2019-166 - Rev 03
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 335
Certificate Number : R1-CEP 2000-099 - Rev 02
Status : Valid
Issue Date : 2017-03-01
Type : Chemical
Substance Number : 335
Certificate Number : CEP 2018-045 - Rev 02
Status : Valid
Issue Date : 2024-10-21
Type : Chemical
Substance Number : 335
Hydrocortisone, Non-micronised, Micronised
Certificate Number : CEP 2019-176 - Rev 01
Status : Valid
Issue Date : 2025-01-17
Type : Chemical
Substance Number : 335
Hydrocortisone, Process B, Micronised, Non-micro...
Certificate Number : R0-CEP 2021-048 - Rev 01
Status : Valid
Issue Date : 2022-05-05
Type : Chemical
Substance Number : 335
Certificate Number : CEP 2017-208 - Rev 01
Status : Valid
Issue Date : 2024-07-19
Type : Chemical
Substance Number : 335
Certificate Number : CEP 2018-239 - Rev 02
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 335
28
PharmaCompass offers a list of Hydrocortisone 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 Hydrocortisone manufacturer or Hydrocortisone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone manufacturer or Hydrocortisone supplier.
PharmaCompass also assists you with knowing the Hydrocortisone API Price utilized in the formulation of products. Hydrocortisone API Price is not always fixed or binding as the Hydrocortisone Price is obtained through a variety of data sources. The Hydrocortisone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Retef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Retef, including repackagers and relabelers. The FDA regulates Retef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Retef 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 Retef manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Retef supplier is an individual or a company that provides Retef active pharmaceutical ingredient (API) or Retef finished formulations upon request. The Retef suppliers may include Retef API manufacturers, exporters, distributors and traders.
click here to find a list of Retef suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Retef CEP of the European Pharmacopoeia monograph is often referred to as a Retef Certificate of Suitability (COS). The purpose of a Retef CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Retef EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Retef to their clients by showing that a Retef CEP has been issued for it. The manufacturer submits a Retef CEP (COS) as part of the market authorization procedure, and it takes on the role of a Retef CEP holder for the record. Additionally, the data presented in the Retef CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Retef DMF.
A Retef CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Retef 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 Retef suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Retef
Get in contact with the supplier of your choice: