01 1Luohe Chief Pharmaceutical Co., Ltd.
01 1Pharmaline Co., Ltd.
01 1Rifabutin
01 1China
Registrant Name : Pharmaline 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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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.
click here to find a list of Prestwick2_001109 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
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, 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 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).
click here to find a list of Prestwick2_001109 suppliers with KDMF on PharmaCompass.
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