01 1Sichuan Xieli Pharmaceutical Co., Ltd.
01 1Pharmapia Co., Ltd.
01 1Troxeroutine
01 1China
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2025-03-11
Registration Number : 20250311-211-J-1805
Manufacturer Name : Sichuan Xieli Pharmaceutical...
Manufacturer Address : No. 588, Middle Section of Mudan Avenue, Tianpeng Town, Pengzhou Sichuan Province, Ch...
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PharmaCompass offers a list of Troxerutin 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 Troxerutin manufacturer or Troxerutin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Troxerutin manufacturer or Troxerutin supplier.
A Venoruton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venoruton, including repackagers and relabelers. The FDA regulates Venoruton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venoruton 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 Venoruton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Venoruton supplier is an individual or a company that provides Venoruton active pharmaceutical ingredient (API) or Venoruton finished formulations upon request. The Venoruton suppliers may include Venoruton API manufacturers, exporters, distributors and traders.
click here to find a list of Venoruton 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 Venoruton Drug Master File in Korea (Venoruton KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Venoruton. The MFDS reviews the Venoruton KDMF as part of the drug registration process and uses the information provided in the Venoruton KDMF to evaluate the safety and efficacy of the drug.
After submitting a Venoruton 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 Venoruton API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Venoruton suppliers with KDMF on PharmaCompass.
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