01 4Pharmacia & Upjohn Company Kalamazoo US
01 11,2-dihydrotriamcinolone
02 1Triamcinolone
03 1Triamcinolone 3, (21-(acetyloxy)pregna-1,4,9(11)-16-tetraene-3,20-dione)
04 1Triamcinolone 5, (9beta,11beta-Epoxy-16alpha,17alpha,21-trihydroxypregna-1,4-diene-3,20-dione)
01 4U.S.A
01 3Expired
02 1Withdrawn by Holder
Triamcinolone 5, (9beta,11beta-Epoxy-16alpha,17a...
Certificate Number : R0-CEP 2001-127 - Rev 00
Status : Expired
Issue Date : 2002-04-09
Type : TSE
Substance Number :
Triamcinolone 3, (21-(acetyloxy)pregna-1,4,9(11)...
Certificate Number : R0-CEP 2001-230 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2002-04-09
Type : TSE
Substance Number :
Certificate Number : R0-CEP 2001-129 - Rev 00
Status : Expired
Issue Date : 2002-05-17
Type : TSE
Substance Number : 1376
Certificate Number : R0-CEP 2001-231 - Rev 00
Status : Expired
Issue Date : 2002-04-09
Type : TSE
Substance Number :
11
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A Adcortyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adcortyl, including repackagers and relabelers. The FDA regulates Adcortyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adcortyl 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 Adcortyl supplier is an individual or a company that provides Adcortyl active pharmaceutical ingredient (API) or Adcortyl finished formulations upon request. The Adcortyl suppliers may include Adcortyl API manufacturers, exporters, distributors and traders.
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A Adcortyl CEP of the European Pharmacopoeia monograph is often referred to as a Adcortyl Certificate of Suitability (COS). The purpose of a Adcortyl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Adcortyl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Adcortyl to their clients by showing that a Adcortyl CEP has been issued for it. The manufacturer submits a Adcortyl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Adcortyl CEP holder for the record. Additionally, the data presented in the Adcortyl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Adcortyl DMF.
A Adcortyl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Adcortyl 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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