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PharmaCompass offers a list of Mometasone Furoate 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 Mometasone Furoate manufacturer or Mometasone Furoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mometasone Furoate manufacturer or Mometasone Furoate supplier.
PharmaCompass also assists you with knowing the Mometasone Furoate API Price utilized in the formulation of products. Mometasone Furoate API Price is not always fixed or binding as the Mometasone Furoate Price is obtained through a variety of data sources. The Mometasone Furoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 04201GDN4R manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04201GDN4R, including repackagers and relabelers. The FDA regulates 04201GDN4R manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04201GDN4R 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 04201GDN4R manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 04201GDN4R supplier is an individual or a company that provides 04201GDN4R active pharmaceutical ingredient (API) or 04201GDN4R finished formulations upon request. The 04201GDN4R suppliers may include 04201GDN4R API manufacturers, exporters, distributors and traders.
click here to find a list of 04201GDN4R 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 04201GDN4R Drug Master File in Japan (04201GDN4R JDMF) empowers 04201GDN4R 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 04201GDN4R JDMF during the approval evaluation for pharmaceutical products. At the time of 04201GDN4R 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 04201GDN4R suppliers with JDMF on PharmaCompass.
We have 4 companies offering 04201GDN4R
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