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Status : Withdrawn by Holder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