01 1Farmabios SpA Gropello Cairoli IT
02 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
03 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
01 2Fluocinolone acetonide
02 1Fluocinolone acetonide, Micronised, non-micronised
01 2China
02 1Gabon
01 3Valid
Certificate Number : R0-CEP 2020-366 - Rev 00
Status : Valid
Issue Date : 2022-08-17
Type : Chemical
Substance Number : 494
Certificate Number : R0-CEP 2021-011 - Rev 00
Status : Valid
Issue Date : 2022-03-21
Type : Chemical
Substance Number : 494
Fluocinolone Acetonide, Micronised, Non-micronis...
Certificate Number : CEP 2004-103 - Rev 03
Status : Valid
Issue Date : 2024-12-02
Type : Chemical
Substance Number : 494
65
PharmaCompass offers a list of Fluocinolone Acetonide 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 Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier.
PharmaCompass also assists you with knowing the Fluocinolone Acetonide API Price utilized in the formulation of products. Fluocinolone Acetonide API Price is not always fixed or binding as the Fluocinolone Acetonide Price is obtained through a variety of data sources. The Fluocinolone Acetonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gelidina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gelidina, including repackagers and relabelers. The FDA regulates Gelidina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gelidina 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 Gelidina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gelidina supplier is an individual or a company that provides Gelidina active pharmaceutical ingredient (API) or Gelidina finished formulations upon request. The Gelidina suppliers may include Gelidina API manufacturers, exporters, distributors and traders.
click here to find a list of Gelidina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gelidina CEP of the European Pharmacopoeia monograph is often referred to as a Gelidina Certificate of Suitability (COS). The purpose of a Gelidina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gelidina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gelidina to their clients by showing that a Gelidina CEP has been issued for it. The manufacturer submits a Gelidina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gelidina CEP holder for the record. Additionally, the data presented in the Gelidina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gelidina DMF.
A Gelidina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gelidina 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 Gelidina suppliers with CEP (COS) on PharmaCompass.
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