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