Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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
01 1Clobetasone butyrate
02 3Clobetasone butyrate, Micronised
01 2India
02 2United Kingdom
01 2Valid
02 2Withdrawn by Holder
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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Status : Withdrawn by Holder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Status : Withdrawn by Holder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
70
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A Clobetasone 17-Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clobetasone 17-Butyrate, including repackagers and relabelers. The FDA regulates Clobetasone 17-Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clobetasone 17-Butyrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Clobetasone 17-Butyrate supplier is an individual or a company that provides Clobetasone 17-Butyrate active pharmaceutical ingredient (API) or Clobetasone 17-Butyrate finished formulations upon request. The Clobetasone 17-Butyrate suppliers may include Clobetasone 17-Butyrate API manufacturers, exporters, distributors and traders.
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A Clobetasone 17-Butyrate CEP of the European Pharmacopoeia monograph is often referred to as a Clobetasone 17-Butyrate Certificate of Suitability (COS). The purpose of a Clobetasone 17-Butyrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clobetasone 17-Butyrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clobetasone 17-Butyrate to their clients by showing that a Clobetasone 17-Butyrate CEP has been issued for it. The manufacturer submits a Clobetasone 17-Butyrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clobetasone 17-Butyrate CEP holder for the record. Additionally, the data presented in the Clobetasone 17-Butyrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clobetasone 17-Butyrate DMF.
A Clobetasone 17-Butyrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clobetasone 17-Butyrate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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