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
29
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nortriptyline manufacturer or Nortriptyline supplier.
A Nortriptyline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nortriptyline Hydrochloride, including repackagers and relabelers. The FDA regulates Nortriptyline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nortriptyline Hydrochloride 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 Nortriptyline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nortriptyline Hydrochloride supplier is an individual or a company that provides Nortriptyline Hydrochloride active pharmaceutical ingredient (API) or Nortriptyline Hydrochloride finished formulations upon request. The Nortriptyline Hydrochloride suppliers may include Nortriptyline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Nortriptyline Hydrochloride 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 Nortriptyline Hydrochloride Drug Master File in Korea (Nortriptyline Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nortriptyline Hydrochloride. The MFDS reviews the Nortriptyline Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Nortriptyline Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nortriptyline Hydrochloride 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 Nortriptyline Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nortriptyline Hydrochloride suppliers with KDMF on PharmaCompass.
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