01 2Nippon Kayaku
01 2Japan
01 2Inactive
01 2Blank
01 2Blank
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6533
Submission : 1986-08-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6537
Submission : 1986-08-12
Status : Inactive
Type : II
A Gusperimus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gusperimus, including repackagers and relabelers. The FDA regulates Gusperimus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gusperimus 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 Gusperimus supplier is an individual or a company that provides Gusperimus active pharmaceutical ingredient (API) or Gusperimus finished formulations upon request. The Gusperimus suppliers may include Gusperimus API manufacturers, exporters, distributors and traders.
click here to find a list of Gusperimus suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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