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PharmaCompass offers a list of Formoterol Fumarate 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 Formoterol Fumarate manufacturer or Formoterol Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Formoterol Fumarate manufacturer or Formoterol Fumarate supplier.
PharmaCompass also assists you with knowing the Formoterol Fumarate API Price utilized in the formulation of products. Formoterol Fumarate API Price is not always fixed or binding as the Formoterol Fumarate Price is obtained through a variety of data sources. The Formoterol Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dulera manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dulera, including repackagers and relabelers. The FDA regulates Dulera manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dulera 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 Dulera manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dulera supplier is an individual or a company that provides Dulera active pharmaceutical ingredient (API) or Dulera finished formulations upon request. The Dulera suppliers may include Dulera API manufacturers, exporters, distributors and traders.
click here to find a list of Dulera 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 Dulera Drug Master File in Japan (Dulera JDMF) empowers Dulera 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 Dulera JDMF during the approval evaluation for pharmaceutical products. At the time of Dulera 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 Dulera suppliers with JDMF on PharmaCompass.
We have 4 companies offering Dulera
Get in contact with the supplier of your choice:
Market Place
Inke S.A: APIs manufacturing plant.
