01 2ACS DOBFAR SPA
01 1Boryeong Co., Ltd.
02 1Sungjin Exim Co., Ltd.
01 2Naphthylin sodium
01 2Italy
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2021-07-08
Registration Number : 20210708-210-J-1060
Manufacturer Name : ACS DOBFAR SPA
Manufacturer Address : Via Rossini, 7/9/11 20067 Tribiano Milano Italy
Registrant Name : Boryeong Co., Ltd.
Registration Date : 2021-07-27
Registration Number : 20210708-210-J-1060(1)
Manufacturer Name : ACS DOBFAR SPA
Manufacturer Address : Via Rossini, 7/9/11 20067 Tribiano Milano Italy
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PharmaCompass offers a list of Nafcillin Sodium 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 Nafcillin Sodium manufacturer or Nafcillin Sodium supplier for your needs.
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A Nallpen In Plastic Container manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nallpen In Plastic Container, including repackagers and relabelers. The FDA regulates Nallpen In Plastic Container manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nallpen In Plastic Container 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 Nallpen In Plastic Container supplier is an individual or a company that provides Nallpen In Plastic Container active pharmaceutical ingredient (API) or Nallpen In Plastic Container finished formulations upon request. The Nallpen In Plastic Container suppliers may include Nallpen In Plastic Container 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 Nallpen In Plastic Container Drug Master File in Korea (Nallpen In Plastic Container KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nallpen In Plastic Container. The MFDS reviews the Nallpen In Plastic Container KDMF as part of the drug registration process and uses the information provided in the Nallpen In Plastic Container KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nallpen In Plastic Container 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 Nallpen In Plastic Container API can apply through the Korea Drug Master File (KDMF).
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