With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Alembic Pharmaceuticals Limited (API Unit-1)
03 1Apitoria Pharma Private Limited (Unit-II)
04 1Apotechnia SA
05 1Asia Chemical Industries Ltd.
06 1Cadila Pharmaceutical Ltd.
07 6Cadila Pharmaceuticals Limited
08 1Cadila Pharmaceuticals Limited_x000D_
09 1Siegfried Ltd
10 1UNION QUIMICO FARMACEUTICA, SA
11 1UNION QUIMICOFARMACEUTICA,SA
12 3Union Quimico Farmaceutica SA
13 6Union Quimico Farmaceutica, SA
14 4Union quimico farmaceutica, SA
With Fermion, start the journey of your innovative API.
Registrant Name : Pharma Science Korea Co., Ltd.
Registration Date : 2014-10-14
Registration Number : 20141014-51-C-327-10
Manufacturer Name : Fermion Oy
Manufacturer Address : Orioninkatu 2, 10900 Hanko, Finland_x000D_
A Fluoxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluoxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Fluoxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluoxetine 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 Fluoxetine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluoxetine Hydrochloride supplier is an individual or a company that provides Fluoxetine Hydrochloride active pharmaceutical ingredient (API) or Fluoxetine Hydrochloride finished formulations upon request. The Fluoxetine Hydrochloride suppliers may include Fluoxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fluoxetine 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 Fluoxetine Hydrochloride Drug Master File in Korea (Fluoxetine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fluoxetine Hydrochloride. The MFDS reviews the Fluoxetine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Fluoxetine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fluoxetine 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 Fluoxetine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fluoxetine Hydrochloride suppliers with KDMF on PharmaCompass.
We have 8 companies offering Fluoxetine Hydrochloride
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