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