01 1Hosho Co
02 1Ohara Pharmaceutical
01 2Japan
01 2Blank
01 2Blank
01 1217MF11219
02 1221MF10217
01 2Blank
Registration Number : 217MF11219
Registrant's Address : 121-15 Toriiino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : --
Registration Number : 221MF10217
Registrant's Address : 7-30-7 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2009-09-30
Latest Date of Registration : --
A Supratonin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Supratonin, including repackagers and relabelers. The FDA regulates Supratonin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Supratonin 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 Supratonin supplier is an individual or a company that provides Supratonin active pharmaceutical ingredient (API) or Supratonin finished formulations upon request. The Supratonin suppliers may include Supratonin API manufacturers, exporters, distributors and traders.
click here to find a list of Supratonin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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