Frovatriptan - NDSRI's

Frovatriptan Nitroso Impurity

  • CAT NUMBER DCTI-C-3066
  • CAS NUMBER NA
  • MOLECULAR FORMULA C14H16N4O2
  • MOLECULAR WEIGHT 272.31
References
FAQ's

Frequently Asked Questions

The impurities in Frovatriptan are monitored during its shelf life to ensure the stability and quality of the medication. Stability testing helps assess their presence and levels over the designated shelf-life period. It ensures that impurity levels remain within acceptable limits and do not increase over time.

Regulatory authorities require manufacturers to provide detailed information about impurities in Frovatriptan as part of the drug approval process. It includes the identification, characterization, and control strategies for impurities. Regulatory agencies review and assess the impurity data to ensure compliance with established guidelines and to verify the safety and quality of Frovatriptan.

Water is the solvent used when analyzing many impurities in Frovatriptan.

The recommendation is to store Frovatriptan impurities at a controlled room temperature, within 2-8 °C.

Note: Products protected by valid patents by a manufacturer are not offered for sale in countries having patent protection. The sale of such products constitutes a patent infringement, and its liability is at the buyer's risk.

Back to Top
Product has been added to your cart