01 1Olon SPA
01 1DKS Korea Co., Ltd.
01 1Mefloquine hydrochloride
01 1Italy
Registrant Name : DKS Korea Co., Ltd.
Registration Date : 2022-09-28
Registration Number : 20220928-209-J-1371
Manufacturer Name : Olon SPA
Manufacturer Address : VIA LIVELLI, 1(loc. FRAZIONE MAIRANO) - 26852 CASALETTO LODIGIANO (LO), Italy
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PharmaCompass offers a list of Mefloquine 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 Mefloquine manufacturer or Mefloquine supplier for your needs.
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PharmaCompass also assists you with knowing the Mefloquine API Price utilized in the formulation of products. Mefloquine API Price is not always fixed or binding as the Mefloquine Price is obtained through a variety of data sources. The Mefloquine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A WR177,602 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of WR177,602, including repackagers and relabelers. The FDA regulates WR177,602 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. WR177,602 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A WR177,602 supplier is an individual or a company that provides WR177,602 active pharmaceutical ingredient (API) or WR177,602 finished formulations upon request. The WR177,602 suppliers may include WR177,602 API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a WR177,602 Drug Master File in Korea (WR177,602 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of WR177,602. The MFDS reviews the WR177,602 KDMF as part of the drug registration process and uses the information provided in the WR177,602 KDMF to evaluate the safety and efficacy of the drug.
After submitting a WR177,602 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 WR177,602 API can apply through the Korea Drug Master File (KDMF).
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