01 1Ash Stevens LLC
02 1Fresenius Kabi Oncology Ltd.
01 1Fresenius Kabi Korea Co., Ltd.
02 1Korea Otsuka Pharmaceutical Co., Ltd.
01 2Attached plate
01 1Sweden
02 1U.S.A
Registrant Name : Korea Otsuka Pharmaceutical Co., Ltd.
Registration Date : 2022-09-26
Registration Number : 20220926-210-J-1369
Manufacturer Name : Ash Stevens LLC
Manufacturer Address : 18655 Krause St., Riverview, MI 48193, USA
Registrant Name : Fresenius Kabi Korea Co., Ltd.
Registration Date : 2018-07-26
Registration Number : 20180726-210-J-248
Manufacturer Name : Fresenius Kabi Oncology Ltd.
Manufacturer Address : D-35, Industrial Area, Kalyani, Dist Nadia, West Bengal, INDIA
85
PharmaCompass offers a list of Busulfan 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 Busulfan manufacturer or Busulfan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Busulfan manufacturer or Busulfan supplier.
A Myelosan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Myelosan, including repackagers and relabelers. The FDA regulates Myelosan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Myelosan 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 Myelosan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Myelosan supplier is an individual or a company that provides Myelosan active pharmaceutical ingredient (API) or Myelosan finished formulations upon request. The Myelosan suppliers may include Myelosan API manufacturers, exporters, distributors and traders.
click here to find a list of Myelosan 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 Myelosan Drug Master File in Korea (Myelosan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Myelosan. The MFDS reviews the Myelosan KDMF as part of the drug registration process and uses the information provided in the Myelosan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Myelosan 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 Myelosan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Myelosan suppliers with KDMF on PharmaCompass.
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