Axplora- The partner of choice for complex APIs.
01 1Farmabios SpA Gropello Cairoli IT
02 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
03 1Pharmacia & Upjohn Company Kalamazoo US
01 2Fludrocortisone acetate
02 1Fludrocortisone acetate, Micronised
01 1China
02 1Italy
03 1U.S.A
01 1Expired
02 2Valid
Axplora- The partner of choice for complex APIs.
Axplora- The partner of choice for complex APIs.
Fludrocortisone Acetate, Micronised
Certificate Number : R0-CEP 2019-084 - Rev 00
Status : Valid
Issue Date : 2020-11-18
Type : Chemical
Substance Number : 767
Certificate Number : CEP 2021-435 - Rev 00
Status : Valid
Issue Date : 2024-05-21
Type : Chemical
Substance Number : 767
Certificate Number : R0-CEP 2001-324 - Rev 00
Status : Expired
Issue Date : 2002-04-09
Type : TSE
Substance Number : 767
A Fludrocortisone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fludrocortisone Acetate, including repackagers and relabelers. The FDA regulates Fludrocortisone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fludrocortisone Acetate 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 Fludrocortisone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fludrocortisone Acetate supplier is an individual or a company that provides Fludrocortisone Acetate active pharmaceutical ingredient (API) or Fludrocortisone Acetate finished formulations upon request. The Fludrocortisone Acetate suppliers may include Fludrocortisone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Fludrocortisone Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fludrocortisone Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Fludrocortisone Acetate Certificate of Suitability (COS). The purpose of a Fludrocortisone Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fludrocortisone Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fludrocortisone Acetate to their clients by showing that a Fludrocortisone Acetate CEP has been issued for it. The manufacturer submits a Fludrocortisone Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fludrocortisone Acetate CEP holder for the record. Additionally, the data presented in the Fludrocortisone Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fludrocortisone Acetate DMF.
A Fludrocortisone Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fludrocortisone Acetate 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 Fludrocortisone Acetate suppliers with CEP (COS) on PharmaCompass.
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