Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
02 1SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
03 3Farmabios SpA Gropello Cairoli IT
04 2EUROAPI FRANCE Vertolaye FR
05 1CURIA SPAIN S.A.U. Boecillo ES
06 1NEWCHEM S.p.A. Milano IT
07 2TIANJIN JINJIN PHARMACEUTICAL CO., LTD. Zhangjiawo Town CN
08 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Hydrocortisone Acetate, Micronised
Certificate Number : CEP 2002-160 - Rev 05
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 334
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Hydrocortisone Acetate, Micronised, Grades I And...
Certificate Number : CEP 2016-228 - Rev 02
Status : Valid
Issue Date : 2023-10-27
Type : Chemical
Substance Number : 334
Axplora is your partner of choice for complex APIs.
Hydrocortisone Acetate, Micronised, Sterile
Certificate Number : R0-CEP 2021-456 - Rev 00
Status : Valid
Issue Date : 2023-04-18
Type : Chemical
Substance Number : 334
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Hydrocortisone Acetate, Micronised
Certificate Number : CEP 1996-053 - Rev 09
Status : Valid
Issue Date : 2024-06-26
Type : Chemical
Substance Number : 334
Axplora is your partner of choice for complex APIs.
Hydrocortisone Acetate, Micronised, Alternative ...
Certificate Number : CEP 2024-068 - Rev 00
Status : Valid
Issue Date : 2024-07-31
Type : Chemical
Substance Number : 334
Axplora is your partner of choice for complex APIs.
Certificate Number : R0-CEP 2020-135 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2020-06-15
Type : Chemical
Substance Number : 334
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Hydrocortisone Acetate, Process 2
Certificate Number : R1-CEP 2012-355 - Rev 01
Status : Valid
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 334
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PharmaCompass offers a list of Hydrocortisone Acetate 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 Acetate manufacturer or Hydrocortisone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier.
PharmaCompass also assists you with knowing the Hydrocortisone Acetate API Price utilized in the formulation of products. Hydrocortisone Acetate API Price is not always fixed or binding as the Hydrocortisone Acetate Price is obtained through a variety of data sources. The Hydrocortisone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PRAMOSONE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PRAMOSONE, including repackagers and relabelers. The FDA regulates PRAMOSONE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PRAMOSONE 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 PRAMOSONE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PRAMOSONE supplier is an individual or a company that provides PRAMOSONE active pharmaceutical ingredient (API) or PRAMOSONE finished formulations upon request. The PRAMOSONE suppliers may include PRAMOSONE API manufacturers, exporters, distributors and traders.
click here to find a list of PRAMOSONE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PRAMOSONE CEP of the European Pharmacopoeia monograph is often referred to as a PRAMOSONE Certificate of Suitability (COS). The purpose of a PRAMOSONE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of PRAMOSONE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of PRAMOSONE to their clients by showing that a PRAMOSONE CEP has been issued for it. The manufacturer submits a PRAMOSONE CEP (COS) as part of the market authorization procedure, and it takes on the role of a PRAMOSONE CEP holder for the record. Additionally, the data presented in the PRAMOSONE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the PRAMOSONE DMF.
A PRAMOSONE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. PRAMOSONE 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 PRAMOSONE suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering PRAMOSONE
Get in contact with the supplier of your choice:
