Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2019-05-20

FDA Approved: SOLIFENACIN SUCCINATE — Original Application (Actavis Pharma, Inc.)

View source ↗

Summary

FDA approved a generic version of solifenacin succinate for overactive bladder under ANDA 202551. Actavis Pharma, Inc. is the applicant.

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

Diseases / indications

Drugs mentioned

  • Solifenacin succinate (solifenacin)

Snippet

ORIG AP for SOLIFENACIN SUCCINATE (SOLIFENACIN SUCCINATE)