Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 2Farmak, as
02 1Apitoria Pharma Private Limited Unit-II
03 1Unichem Laboratories Limited
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registrant Name : Ankuk Pharmaceutical Co., Ltd.
Registration Date : 2020-07-02
Registration Number : 20200115-209-J-260(1)
Manufacturer Name : Farmak, as
Manufacturer Address : Na vlcinci 16/3, Klasterni Hradisko, 779 00 Olomouc, Czech Republic
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registrant Name : Iksoo Pharmaceutical Co., Ltd.
Registration Date : 2020-01-15
Registration Number : 20200115-209-J-260
Manufacturer Name : Farmak, as
Manufacturer Address : Na vlcinci 16/3, Klasterni Hradisko, 779 00 Olomouc, Czech Republic
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PharmaCompass offers a list of Alfuzosin HCl 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 Alfuzosin HCl manufacturer or Alfuzosin HCl supplier for your needs.
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A Xatral XL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xatral XL, including repackagers and relabelers. The FDA regulates Xatral XL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xatral XL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Xatral XL supplier is an individual or a company that provides Xatral XL active pharmaceutical ingredient (API) or Xatral XL finished formulations upon request. The Xatral XL suppliers may include Xatral XL API manufacturers, exporters, distributors and traders.
click here to find a list of Xatral XL 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 Xatral XL Drug Master File in Korea (Xatral XL KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Xatral XL. The MFDS reviews the Xatral XL KDMF as part of the drug registration process and uses the information provided in the Xatral XL KDMF to evaluate the safety and efficacy of the drug.
After submitting a Xatral XL 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 Xatral XL API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Xatral XL suppliers with KDMF on PharmaCompass.
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