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Status : Withdrawn by Holder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 Kenacort manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kenacort, including repackagers and relabelers. The FDA regulates Kenacort manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kenacort 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 Kenacort supplier is an individual or a company that provides Kenacort active pharmaceutical ingredient (API) or Kenacort finished formulations upon request. The Kenacort suppliers may include Kenacort API manufacturers, exporters, distributors and traders.
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A Kenacort CEP of the European Pharmacopoeia monograph is often referred to as a Kenacort Certificate of Suitability (COS). The purpose of a Kenacort CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Kenacort EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Kenacort to their clients by showing that a Kenacort CEP has been issued for it. The manufacturer submits a Kenacort CEP (COS) as part of the market authorization procedure, and it takes on the role of a Kenacort CEP holder for the record. Additionally, the data presented in the Kenacort CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Kenacort DMF.
A Kenacort CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Kenacort 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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