Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
02 1AVIK PHARMACEUTICAL LIMITED Vapi IN
03 1GlaxoSmithKline Research & Development Limited Brentford GB
04 1GlaxoSmithKline Research & Development Limited London GB
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01 1Clobetasone butyrate
02 3Clobetasone butyrate, Micronised
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01 2India
02 2United Kingdom
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01 2Valid
02 2Withdrawn by Holder
Clobetasone Butyrate, Micronised
Certificate Number : R1-CEP 2012-282 - Rev 00
Status : Valid
Issue Date : 2019-10-17
Type : Chemical
Substance Number : 1090
Certificate Number : CEP 2018-105 - Rev 01
Status : Valid
Issue Date : 2024-10-29
Type : Chemical
Substance Number : 1090
Clobetasone Butyrate, Micronised
Certificate Number : R1-CEP 2002-248 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2015-04-13
Type : Chemical
Substance Number : 1090
Clobetasone Butyrate, Micronised
Certificate Number : R1-CEP 2006-186 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2013-08-06
Type : Chemical
Substance Number : 1090
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PharmaCompass offers a list of Clobetasone Butyrate 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 Clobetasone Butyrate manufacturer or Clobetasone Butyrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clobetasone Butyrate manufacturer or Clobetasone Butyrate supplier.
PharmaCompass also assists you with knowing the Clobetasone Butyrate API Price utilized in the formulation of products. Clobetasone Butyrate API Price is not always fixed or binding as the Clobetasone Butyrate Price is obtained through a variety of data sources. The Clobetasone Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Emovate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emovate, including repackagers and relabelers. The FDA regulates Emovate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emovate 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 Emovate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Emovate supplier is an individual or a company that provides Emovate active pharmaceutical ingredient (API) or Emovate finished formulations upon request. The Emovate suppliers may include Emovate API manufacturers, exporters, distributors and traders.
click here to find a list of Emovate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Emovate CEP of the European Pharmacopoeia monograph is often referred to as a Emovate Certificate of Suitability (COS). The purpose of a Emovate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Emovate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Emovate to their clients by showing that a Emovate CEP has been issued for it. The manufacturer submits a Emovate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Emovate CEP holder for the record. Additionally, the data presented in the Emovate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Emovate DMF.
A Emovate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Emovate 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 Emovate suppliers with CEP (COS) on PharmaCompass.
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