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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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a VIMOVO Drug Master File in Korea (VIMOVO KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of VIMOVO. The MFDS reviews the VIMOVO KDMF as part of the drug registration process and uses the information provided in the VIMOVO KDMF to evaluate the safety and efficacy of the drug.
After submitting a VIMOVO KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their VIMOVO API can apply through the Korea Drug Master File (KDMF).
click here to find a list of VIMOVO suppliers with KDMF on PharmaCompass.
We have 24 companies offering VIMOVO
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