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