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