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PharmaCompass offers a list of Duloxetine 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 Duloxetine manufacturer or Duloxetine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Duloxetine manufacturer or Duloxetine supplier.
PharmaCompass also assists you with knowing the Duloxetine API Price utilized in the formulation of products. Duloxetine API Price is not always fixed or binding as the Duloxetine Price is obtained through a variety of data sources. The Duloxetine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cymbalta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cymbalta, including repackagers and relabelers. The FDA regulates Cymbalta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cymbalta API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cymbalta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cymbalta supplier is an individual or a company that provides Cymbalta active pharmaceutical ingredient (API) or Cymbalta finished formulations upon request. The Cymbalta suppliers may include Cymbalta API manufacturers, exporters, distributors and traders.
click here to find a list of Cymbalta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cymbalta CEP of the European Pharmacopoeia monograph is often referred to as a Cymbalta Certificate of Suitability (COS). The purpose of a Cymbalta CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cymbalta EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cymbalta to their clients by showing that a Cymbalta CEP has been issued for it. The manufacturer submits a Cymbalta CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cymbalta CEP holder for the record. Additionally, the data presented in the Cymbalta CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cymbalta DMF.
A Cymbalta CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cymbalta 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 Cymbalta suppliers with CEP (COS) on PharmaCompass.
We have 25 companies offering Cymbalta
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