Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
01 1EGIS Pharmaceuticals Plc.
02 1Harman Finochem Limited
03 1SMS Lifesciences India Limited
01 1Masung LS Co., Ltd.
02 1Pharmapia Co., Ltd.
03 1Samil Pharmaceutical Co., Ltd.
01 3Allopurinol
01 1Hungary
02 2India
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2021-01-25
Registration Number : 20210125-209-J-511
Manufacturer Name : EGIS Pharmaceuticals Plc.
Manufacturer Address : Kereszturi ut 30-38., Budapest, 1106, Hungary
Registrant Name : Samil Pharmaceutical Co., Ltd.
Registration Date : 2021-04-20
Registration Number : 20210420-209-J-559
Manufacturer Name : Harman Finochem Limited
Manufacturer Address : A-100, A-100/1, A-100/2 & D-1, MIDC Industrial Area, Shendra, Aurangabad -431 007, Ma...
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2021-12-02
Registration Number : 20211202-209-J-1166
Manufacturer Name : SMS Lifesciences India Limit...
Manufacturer Address : Unit-I, Sy No. 180/2, Kazipalli (V), Jinnaram (M), Sangareddy District, Telangana - 5...
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PharmaCompass offers a list of Allopurinol 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 Allopurinol manufacturer or Allopurinol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Allopurinol manufacturer or Allopurinol supplier.
A Xanthomax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xanthomax, including repackagers and relabelers. The FDA regulates Xanthomax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xanthomax 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 Xanthomax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Xanthomax supplier is an individual or a company that provides Xanthomax active pharmaceutical ingredient (API) or Xanthomax finished formulations upon request. The Xanthomax suppliers may include Xanthomax API manufacturers, exporters, distributors and traders.
click here to find a list of Xanthomax 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 Xanthomax Drug Master File in Korea (Xanthomax KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Xanthomax. The MFDS reviews the Xanthomax KDMF as part of the drug registration process and uses the information provided in the Xanthomax KDMF to evaluate the safety and efficacy of the drug.
After submitting a Xanthomax 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 Xanthomax API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Xanthomax suppliers with KDMF on PharmaCompass.
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