Catalyst Wire Dossier Catalyst Wire Dossier
FDA label_change · 2011-04-25

FDA Approved: ZARONTIN — Supplemental Application (Parke-Davis Div of Pfizer Inc)

View source ↗

Summary

FDA approves a supplemental application for Zarontin (ethosuximide) from Parke-Davis Div of Pfizer to update the product labeling.

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

Diseases / indications

Drugs mentioned

  • ZARONTIN (ethosuximide)

Snippet

SUPPL AP for ZARONTIN (ETHOSUXIMIDE)