01 2Procos SPA
01 1Ace Biopharm Co., Ltd.
02 1Sungjin Exim Co., Ltd.
01 2Napronil oxalate
01 2Italy
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2021-03-23
Registration Number : 20210323-211-J-895
Manufacturer Name : Procos SPA
Manufacturer Address : Viamatteotti 249, Cameri(Novara)28062 Italy
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2021-05-18
Registration Number : 20210323-211-J-895(1)
Manufacturer Name : Procos SPA
Manufacturer Address : Viamatteotti 249, Cameri(Novara)28062 Italy
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PharmaCompass offers a list of Nafronyl Oxalate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Nafronyl Oxalate manufacturer or Nafronyl Oxalate supplier for your needs.
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A Naftilong manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naftilong, including repackagers and relabelers. The FDA regulates Naftilong manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naftilong 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 Naftilong manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Naftilong supplier is an individual or a company that provides Naftilong active pharmaceutical ingredient (API) or Naftilong finished formulations upon request. The Naftilong suppliers may include Naftilong API manufacturers, exporters, distributors and traders.
click here to find a list of Naftilong suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Naftilong Drug Master File in Korea (Naftilong KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Naftilong. The MFDS reviews the Naftilong KDMF as part of the drug registration process and uses the information provided in the Naftilong KDMF to evaluate the safety and efficacy of the drug.
After submitting a Naftilong 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 Naftilong API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Naftilong suppliers with KDMF on PharmaCompass.
