01 1Lusochimica SpA
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Nimodipine
01 1Italy
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2021-03-10
Registration Number : 20210310-209-J-534
Manufacturer Name : Lusochimica SpA
Manufacturer Address : Via Giotto 9, 23871 Lomagna (LC), Italy
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PharmaCompass offers a list of Nimodipine 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 Nimodipine manufacturer or Nimodipine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nimodipine manufacturer or Nimodipine supplier.
A Nimodipino manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nimodipino, including repackagers and relabelers. The FDA regulates Nimodipino manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nimodipino 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 Nimodipino manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nimodipino supplier is an individual or a company that provides Nimodipino active pharmaceutical ingredient (API) or Nimodipino finished formulations upon request. The Nimodipino suppliers may include Nimodipino API manufacturers, exporters, distributors and traders.
click here to find a list of Nimodipino 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 Nimodipino Drug Master File in Korea (Nimodipino KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nimodipino. The MFDS reviews the Nimodipino KDMF as part of the drug registration process and uses the information provided in the Nimodipino KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nimodipino 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 Nimodipino API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nimodipino suppliers with KDMF on PharmaCompass.
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