01 3chemical factory berg GmbH
02 1chemische fabrication berk GmbH
03 2Olon SpA
04 2Sun Pharmaceutical Industries Ltd
05 2Sun Pharmaceutical Industries Ltd.
Registrant Name : Korea BMI Co., Ltd.
Registration Date : 2013-07-15
Registration Number : 20080331-98-E-32-03(5)
Manufacturer Name : chemical factory berg GmbH
Manufacturer Address : Mainthalstrasse 3 D-06749 Bitterfeld
Registrant Name : Koojoo Pharmaceutical Co., Ltd.
Registration Date : 2011-10-21
Registration Number : 20080331-98-E-32-03(1)
Manufacturer Name : chemische fabrication berk G...
Manufacturer Address : Mainthalstrasse 3 D-06749 bitterfeld
Registrant Name : Hyons Co., Ltd.
Registration Date : 2008-03-31
Registration Number : 20080331-98-E-32-03
Manufacturer Name : chemical factory berg GmbH
Manufacturer Address : Mainthalstrasse 3 D-06749 bitterfeld
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2013-02-14
Registration Number : 20080331-98-E-32-03(4)
Manufacturer Name : chemical factory berg GmbH
Manufacturer Address : Mainthalstrasse 3 D-06749 bitterfeld
74
PharmaCompass offers a list of Phentermine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Phentermine Hydrochloride manufacturer or Phentermine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phentermine Hydrochloride manufacturer or Phentermine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Phentermine Hydrochloride API Price utilized in the formulation of products. Phentermine Hydrochloride API Price is not always fixed or binding as the Phentermine Hydrochloride Price is obtained through a variety of data sources. The Phentermine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A QSYMIA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QSYMIA, including repackagers and relabelers. The FDA regulates QSYMIA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QSYMIA 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 QSYMIA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A QSYMIA supplier is an individual or a company that provides QSYMIA active pharmaceutical ingredient (API) or QSYMIA finished formulations upon request. The QSYMIA suppliers may include QSYMIA API manufacturers, exporters, distributors and traders.
click here to find a list of QSYMIA 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 QSYMIA Drug Master File in Korea (QSYMIA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of QSYMIA. The MFDS reviews the QSYMIA KDMF as part of the drug registration process and uses the information provided in the QSYMIA KDMF to evaluate the safety and efficacy of the drug.
After submitting a QSYMIA 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 QSYMIA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of QSYMIA suppliers with KDMF on PharmaCompass.
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