01 1Luohe Chief Pharmaceutical Co., Ltd.
01 1Parmarine Co., Ltd.
01 1Rifabutin
01 1China
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2025-02-28
Registration Number : 20250228-209-J-1778
Manufacturer Name : Luohe Chief Pharmaceutical C...
Manufacturer Address : No.168, Longjiang Road, Yancheng District, Luohe City, Henan Province, 462300 PR Chin...
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PharmaCompass offers a list of Rifabutin 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 Rifabutin manufacturer or Rifabutin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rifabutin manufacturer or Rifabutin supplier.
PharmaCompass also assists you with knowing the Rifabutin API Price utilized in the formulation of products. Rifabutin API Price is not always fixed or binding as the Rifabutin Price is obtained through a variety of data sources. The Rifabutin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prestwick2_001109 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick2_001109, including repackagers and relabelers. The FDA regulates Prestwick2_001109 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick2_001109 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 Prestwick2_001109 supplier is an individual or a company that provides Prestwick2_001109 active pharmaceutical ingredient (API) or Prestwick2_001109 finished formulations upon request. The Prestwick2_001109 suppliers may include Prestwick2_001109 API manufacturers, exporters, distributors and traders.
click here to find a list of Prestwick2_001109 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 Prestwick2_001109 Drug Master File in Korea (Prestwick2_001109 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Prestwick2_001109. The MFDS reviews the Prestwick2_001109 KDMF as part of the drug registration process and uses the information provided in the Prestwick2_001109 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Prestwick2_001109 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 Prestwick2_001109 API can apply through the Korea Drug Master File (KDMF).
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