01 1Dipharma Francis Srl
01 1Masung LS Co., Ltd.
01 1Selegiline hydrochloride
01 1Italy
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2021-08-19
Registration Number : 20210819-209-J-950
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via Bissone 5 20021 Baranzate (MI), Italy
25
PharmaCompass offers a list of Selegiline Hydrochloride 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 Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier.
A L-Deprenyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Deprenyl, including repackagers and relabelers. The FDA regulates L-Deprenyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Deprenyl 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 L-Deprenyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A L-Deprenyl supplier is an individual or a company that provides L-Deprenyl active pharmaceutical ingredient (API) or L-Deprenyl finished formulations upon request. The L-Deprenyl suppliers may include L-Deprenyl API manufacturers, exporters, distributors and traders.
click here to find a list of L-Deprenyl 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 L-Deprenyl Drug Master File in Korea (L-Deprenyl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of L-Deprenyl. The MFDS reviews the L-Deprenyl KDMF as part of the drug registration process and uses the information provided in the L-Deprenyl KDMF to evaluate the safety and efficacy of the drug.
After submitting a L-Deprenyl 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 L-Deprenyl API can apply through the Korea Drug Master File (KDMF).
click here to find a list of L-Deprenyl suppliers with KDMF on PharmaCompass.
