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Status : Withdrawn by Holder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