Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2023-01-31

FDA Approved: IMATINIB MESYLATE — Supplemental Application (BluePoint Laboratories)

View source ↗

Summary

FDA approves a supplemental application for Imatinib Mesylate from BluePoint Laboratories under an ANDA, confirming approval of a generic product. The drug is i…

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

Diseases / indications

Drugs mentioned

  • Imatinib mesylate (Imatinib)

Snippet

SUPPL AP for IMATINIB MESYLATE (IMATINIB MESYLATE)