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PharmaCompass offers a list of Raloxifene Hydrochloride 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 Raloxifene Hydrochloride manufacturer or Raloxifene Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Raloxifene Hydrochloride manufacturer or Raloxifene Hydrochloride supplier.
PharmaCompass also assists you with knowing the Raloxifene Hydrochloride API Price utilized in the formulation of products. Raloxifene Hydrochloride API Price is not always fixed or binding as the Raloxifene Hydrochloride Price is obtained through a variety of data sources. The Raloxifene Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Evista manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Evista, including repackagers and relabelers. The FDA regulates Evista manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Evista 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 Evista manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Evista supplier is an individual or a company that provides Evista active pharmaceutical ingredient (API) or Evista finished formulations upon request. The Evista suppliers may include Evista API manufacturers, exporters, distributors and traders.
click here to find a list of Evista 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 Evista Drug Master File in Korea (Evista KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Evista. The MFDS reviews the Evista KDMF as part of the drug registration process and uses the information provided in the Evista KDMF to evaluate the safety and efficacy of the drug.
After submitting a Evista 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 Evista API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Evista suppliers with KDMF on PharmaCompass.
We have 6 companies offering Evista
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