01 1Olon SpA
02 1Samhwa Biopharm Co., Ltd.
01 1Sam-O Pharmaceutical Co., Ltd.
02 1Samhwa Biopharm Co., Ltd.
01 2Diethylpropion hydrochloride
01 1Italy
02 1South Korea
Registrant Name : Samhwa Biopharm Co., Ltd.
Registration Date : 2009-06-17
Registration Number : 20090617-97-E-84-02
Manufacturer Name : Samhwa Biopharm Co., Ltd.
Manufacturer Address : 150 Hyeopnyeop-ro, Siheung-si, Gyeonggi-do
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2008-02-05
Registration Number : 20080204-97-E-39-01
Manufacturer Name : Olon SpA
Manufacturer Address : Via Milano, 186 20024 Garbagnate Milanese (MI), Italy
82
PharmaCompass offers a list of Diethylpropion 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 Diethylpropion Hydrochloride manufacturer or Diethylpropion Hydrochloride supplier for your needs.
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A Magrex Retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magrex Retard, including repackagers and relabelers. The FDA regulates Magrex Retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magrex Retard 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 Magrex Retard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Magrex Retard supplier is an individual or a company that provides Magrex Retard active pharmaceutical ingredient (API) or Magrex Retard finished formulations upon request. The Magrex Retard suppliers may include Magrex Retard API manufacturers, exporters, distributors and traders.
click here to find a list of Magrex Retard 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 Magrex Retard Drug Master File in Korea (Magrex Retard KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Magrex Retard. The MFDS reviews the Magrex Retard KDMF as part of the drug registration process and uses the information provided in the Magrex Retard KDMF to evaluate the safety and efficacy of the drug.
After submitting a Magrex Retard 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 Magrex Retard API can apply through the Korea Drug Master File (KDMF).
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