01 1Zydus Lifesciences Limited
01 1MPK Korea Co., Ltd.
01 1Benzoyl peroxide
01 1India
Registrant Name : MPK Korea Co., Ltd.
Registration Date : 2025-09-16
Registration Number : 20250916-211-J-2023
Manufacturer Name : Zydus Lifesciences Limited
Manufacturer Address : Plot No. 291, GIDC Estate, City - Ankleshwar - 393 002, Dist. - Bharuch, Gujarat Stat...
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PharmaCompass offers a list of Benzoyl Peroxide 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 Benzoyl Peroxide manufacturer or Benzoyl Peroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzoyl Peroxide manufacturer or Benzoyl Peroxide supplier.
A Quinolor compound manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinolor compound, including repackagers and relabelers. The FDA regulates Quinolor compound manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinolor compound 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 Quinolor compound manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Quinolor compound supplier is an individual or a company that provides Quinolor compound active pharmaceutical ingredient (API) or Quinolor compound finished formulations upon request. The Quinolor compound suppliers may include Quinolor compound API manufacturers, exporters, distributors and traders.
click here to find a list of Quinolor compound 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 Quinolor compound Drug Master File in Korea (Quinolor compound KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Quinolor compound. The MFDS reviews the Quinolor compound KDMF as part of the drug registration process and uses the information provided in the Quinolor compound KDMF to evaluate the safety and efficacy of the drug.
After submitting a Quinolor compound 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 Quinolor compound API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Quinolor compound suppliers with KDMF on PharmaCompass.
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