01 1Pharmacia & Upjohn Company Kalamazoo US
01 1Triamcinolone-21-acetate
01 1U.S.A
01 1Expired
Certificate Number : R0-CEP 2001-069 - Rev 00
Status : Expired
Issue Date : 2002-05-29
Type : TSE
Substance Number :
43
PharmaCompass offers a list of Triamcinolone Diacetate 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 Diacetate manufacturer or Triamcinolone Diacetate supplier for your needs.
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PharmaCompass also assists you with knowing the Triamcinolone Diacetate API Price utilized in the formulation of products. Triamcinolone Diacetate API Price is not always fixed or binding as the Triamcinolone Diacetate Price is obtained through a variety of data sources. The Triamcinolone Diacetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Triamcinolone Diacetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triamcinolone Diacetate, including repackagers and relabelers. The FDA regulates Triamcinolone Diacetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triamcinolone Diacetate 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 Triamcinolone Diacetate supplier is an individual or a company that provides Triamcinolone Diacetate active pharmaceutical ingredient (API) or Triamcinolone Diacetate finished formulations upon request. The Triamcinolone Diacetate suppliers may include Triamcinolone Diacetate API manufacturers, exporters, distributors and traders.
click here to find a list of Triamcinolone Diacetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Triamcinolone Diacetate CEP of the European Pharmacopoeia monograph is often referred to as a Triamcinolone Diacetate Certificate of Suitability (COS). The purpose of a Triamcinolone Diacetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Triamcinolone Diacetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Triamcinolone Diacetate to their clients by showing that a Triamcinolone Diacetate CEP has been issued for it. The manufacturer submits a Triamcinolone Diacetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Triamcinolone Diacetate CEP holder for the record. Additionally, the data presented in the Triamcinolone Diacetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Triamcinolone Diacetate DMF.
A Triamcinolone Diacetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Triamcinolone Diacetate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Triamcinolone Diacetate suppliers with CEP (COS) on PharmaCompass.
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