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