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Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide. 
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01 Pharmaceutical Works POLPHARMA S. A. (1)
02 PLIVA CROATIA LTD. (1)
01 Etodolac (1)
02 Etodolac "Teva / PLIVA2" (1)
01 Croatia (1)
02 Poland (1)
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PharmaCompass offers a list of Etodolac 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 Etodolac manufacturer or Etodolac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etodolac manufacturer or Etodolac supplier.
PharmaCompass also assists you with knowing the Etodolac API Price utilized in the formulation of products. Etodolac API Price is not always fixed or binding as the Etodolac Price is obtained through a variety of data sources. The Etodolac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etoflam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etoflam, including repackagers and relabelers. The FDA regulates Etoflam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etoflam 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 Etoflam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etoflam supplier is an individual or a company that provides Etoflam active pharmaceutical ingredient (API) or Etoflam finished formulations upon request. The Etoflam suppliers may include Etoflam API manufacturers, exporters, distributors and traders.
click here to find a list of Etoflam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Etoflam Drug Master File in Japan (Etoflam JDMF) empowers Etoflam API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Etoflam JDMF during the approval evaluation for pharmaceutical products. At the time of Etoflam JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Etoflam suppliers with JDMF on PharmaCompass.
We have 2 companies offering Etoflam
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