01 1Dipharma Francis Srl
01 1Toru Co., Ltd.
01 1nortriptyline hydrochloride
01 1Italy
Registrant Name : Toru Co., Ltd.
Registration Date : 2024-11-12
Registration Number : 20241112-209-J-1722
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via Bissone, 5, 20021, Baranzate (MI), Italy
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PharmaCompass offers a list of Nortriptyline 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 Nortriptyline manufacturer or Nortriptyline supplier for your needs.
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A Aventyl allegron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aventyl allegron, including repackagers and relabelers. The FDA regulates Aventyl allegron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aventyl allegron 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 Aventyl allegron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Aventyl allegron supplier is an individual or a company that provides Aventyl allegron active pharmaceutical ingredient (API) or Aventyl allegron finished formulations upon request. The Aventyl allegron suppliers may include Aventyl allegron API manufacturers, exporters, distributors and traders.
click here to find a list of Aventyl allegron 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 Aventyl allegron Drug Master File in Korea (Aventyl allegron KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Aventyl allegron. The MFDS reviews the Aventyl allegron KDMF as part of the drug registration process and uses the information provided in the Aventyl allegron KDMF to evaluate the safety and efficacy of the drug.
After submitting a Aventyl allegron 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 Aventyl allegron API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Aventyl allegron suppliers with KDMF on PharmaCompass.
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