01 Helsinn Advanced Synthesis SA (Helsinn/HAS) (1)
02 Mangalam Drugs and Organics Ltd. (Unit-2) (1)
01 Ace Biopharm Co., Ltd. (1)
02 JW Pharmaceutical Co., Ltd. (1)
01 Nimesulid (2)
01 India (1)
02 Switzerland (1)
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PharmaCompass offers a list of Nimesulide 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 Nimesulide manufacturer or Nimesulide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nimesulide manufacturer or Nimesulide supplier.
PharmaCompass also assists you with knowing the Nimesulide API Price utilized in the formulation of products. Nimesulide API Price is not always fixed or binding as the Nimesulide Price is obtained through a variety of data sources. The Nimesulide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Redaflam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Redaflam, including repackagers and relabelers. The FDA regulates Redaflam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Redaflam 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 Redaflam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Redaflam supplier is an individual or a company that provides Redaflam active pharmaceutical ingredient (API) or Redaflam finished formulations upon request. The Redaflam suppliers may include Redaflam API manufacturers, exporters, distributors and traders.
click here to find a list of Redaflam 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 Redaflam Drug Master File in Korea (Redaflam KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Redaflam. The MFDS reviews the Redaflam KDMF as part of the drug registration process and uses the information provided in the Redaflam KDMF to evaluate the safety and efficacy of the drug.
After submitting a Redaflam 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 Redaflam API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Redaflam suppliers with KDMF on PharmaCompass.
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