01 3chemical factory berg GmbH
02 1chemical factory 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 : chemical factory berk GmbH
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
90
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 LOMAIRA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LOMAIRA, including repackagers and relabelers. The FDA regulates LOMAIRA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LOMAIRA 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 LOMAIRA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LOMAIRA supplier is an individual or a company that provides LOMAIRA active pharmaceutical ingredient (API) or LOMAIRA finished formulations upon request. The LOMAIRA suppliers may include LOMAIRA API manufacturers, exporters, distributors and traders.
click here to find a list of LOMAIRA 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 LOMAIRA Drug Master File in Korea (LOMAIRA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of LOMAIRA. The MFDS reviews the LOMAIRA KDMF as part of the drug registration process and uses the information provided in the LOMAIRA KDMF to evaluate the safety and efficacy of the drug.
After submitting a LOMAIRA 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 LOMAIRA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of LOMAIRA suppliers with KDMF on PharmaCompass.
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