01 1Pharmacostech
02 1Yamasa Corporation
01 1Japan
02 1South Korea
01 2Blank
01 2Blank
01 1221MF10012
02 1221MF10052
01 2Blank
Registration Number : 221MF10012
Registrant's Address : 47, Jeyakdanji-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Republic of Korea
Initial Date of Registration : 2009-01-13
Latest Date of Registration : --
Registration Number : 221MF10052
Registrant's Address : 2-10-1 Shinseicho, Choshi City, Chiba Prefecture
Initial Date of Registration : 2009-03-16
Latest Date of Registration : --
A Mizoribine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mizoribine, including repackagers and relabelers. The FDA regulates Mizoribine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mizoribine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Mizoribine supplier is an individual or a company that provides Mizoribine active pharmaceutical ingredient (API) or Mizoribine finished formulations upon request. The Mizoribine suppliers may include Mizoribine API manufacturers, exporters, distributors and traders.
click here to find a list of Mizoribine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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