Catalyst Wire Dossier Catalyst Wire Dossier
FDA label_change · 2014-05-06

FDA Approved: PROCARDIA XL — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)

View source ↗

Summary

FDA approved a supplemental application for Procardia XL (nifedipine) from Pfizer Laboratories to update the product labeling.

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

Diseases / indications

Drugs mentioned

  • PROCARDIA XL (NIFEDIPINE)

Snippet

SUPPL AP for PROCARDIA XL (NIFEDIPINE)