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