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PharmaCompass offers a list of Minoxidil 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 Minoxidil manufacturer or Minoxidil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Minoxidil manufacturer or Minoxidil supplier.
PharmaCompass also assists you with knowing the Minoxidil API Price utilized in the formulation of products. Minoxidil API Price is not always fixed or binding as the Minoxidil Price is obtained through a variety of data sources. The Minoxidil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prexidil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prexidil, including repackagers and relabelers. The FDA regulates Prexidil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prexidil 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 Prexidil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prexidil supplier is an individual or a company that provides Prexidil active pharmaceutical ingredient (API) or Prexidil finished formulations upon request. The Prexidil suppliers may include Prexidil API manufacturers, exporters, distributors and traders.
click here to find a list of Prexidil 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 Prexidil Drug Master File in Korea (Prexidil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Prexidil. The MFDS reviews the Prexidil KDMF as part of the drug registration process and uses the information provided in the Prexidil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Prexidil 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 Prexidil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Prexidil suppliers with KDMF on PharmaCompass.
We have 3 companies offering Prexidil
Get in contact with the supplier of your choice: