Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2022-10-31

FDA Approved: BONJESTA — Supplemental Application (Duchesnay USA, Inc.)

View source ↗

Summary

The FDA approved a supplemental application for Bonjesta (doxylamine succinate and pyridoxine hydrochloride) submitted by Duchesnay USA, Inc., under NDA 209661.

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • Bonjesta (doxylamine succinate and pyridoxine hydrochloride)

Snippet

SUPPL AP for BONJESTA (DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE)